Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation (Q42930492)

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scientific article published on 3 August 2010

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English	Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation	scientific article published on 3 August 2010

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scholarly article

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Europe PubMed Central

PubMed publication ID

11 November 2017

Mitochondrial haplogroup M9a specific variant ND1 T3394C may have a modifying role in the phenotypic expression of the LHON-associated ND4 G11778A mutation (English)

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Europe PubMed Central

PubMed publication ID

11 November 2017

author name string

Minglian Zhang

1

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11 November 2017

Xiangtian Zhou

2

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11 November 2017

Chengwu Li

3

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11 November 2017

Fuxin Zhao

4

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11 November 2017

Juanjuan Zhang

5

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11 November 2017

Meixia Yuan

6

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11 November 2017

Yan-Hong Sun

7

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11 November 2017

Jingzheng Wang

8

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11 November 2017

Yi Tong

9

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11 November 2017

Min Liang

10

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11 November 2017

Li Yang

11

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11 November 2017

Wanshi Cai

12

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11 November 2017

Lifei Wang

13

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11 November 2017

Jia Qu

14

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11 November 2017

Min-Xin Guan

15

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11 November 2017

publication date

3 August 2010

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11 November 2017

Molecular Genetics and Metabolism

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11 November 2017

101

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11 November 2017

2-3

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11 November 2017

192-199

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11 November 2017

Inherited mitochondrial optic neuropathies

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

LHON and other optic nerve atrophies: the mitochondrial connection

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Mitochondrial encephalomyopathies: gene mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

MITOMAP: a human mitochondrial genome database--2004 update

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Spectrum of pathogenic mitochondrial DNA mutations and clinical features in Japanese families with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

1 reference

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7 January 2021

Retinal ganglion cell neurodegeneration in mitochondrial inherited disorders

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https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Molecular epidemiology of mtDNA mutations in 903 Chinese families suspected with Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

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Genome-wide linkage scan and association study of PARL to the expression of LHON families in Thailand

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

The novel A4435G mutation in the mitochondrial tRNAMet may modulate the phenotypic expression of the LHON-associated ND4 G11778A mutation

1 reference

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7 January 2021

The mitochondrial tRNA(Thr) A15951G mutation may influence the phenotypic expression of the LHON-associated ND4 G11778A mutation in a Chinese family.

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Cosegregation of the ND4 G11696A mutation with the LHON-associated ND4 G11778A mutation in a four generation Chinese family

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Mitochondrial variants may influence the phenotypic manifestation of Leber's hereditary optic neuropathy-associated ND4 G11778A mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Extremely low penetrance of Leber's hereditary optic neuropathy in 8 Han Chinese families carrying the ND4 G11778A mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Only male matrilineal relatives with Leber's hereditary optic neuropathy in a large Chinese family carrying the mitochondrial DNA G11778A mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Clinical evaluation and mitochondrial DNA sequence analysis in three Chinese families with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Leber's hereditary optic neuropathy is associated with mitochondrial ND1 T3394C mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Automating the identification of DNA variations using quality-based fluorescence re-sequencing: analysis of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Mitochondrial genome variation in eastern Asia and the peopling of Japan

1 reference

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7 January 2021

Updating the East Asian mtDNA phylogeny: a prerequisite for the identification of pathogenic mutations

1 reference

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7 January 2021

Epidemiology and penetrance of Leber hereditary optic neuropathy in Finland

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https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Comprehensive association testing of common mitochondrial DNA variation in metabolic disease

1 reference

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7 January 2021

Mutations at position 7445 in the precursor of mitochondrial tRNA(Ser(UCN)) gene in three maternal Chinese pedigrees with sensorineural hearing loss

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Sequence and gene organization of mouse mitochondrial DNA

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7 January 2021

The complete nucleotide sequence of the Rattus norvegicus mitochondrial genome: cryptic signals revealed by comparative analysis between vertebrates

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Ophthalmologic findings in Leber hereditary optic neuropathy, with special reference to mtDNA mutations

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Leber's hereditary optic neuropathy affects only female matrilineal relatives in two Chinese families

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Very high penetrance and occurrence of Leber's hereditary optic neuropathy in a large Han Chinese pedigree carrying the ND4 G11778A mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

X chromosome-linked and mitochondrial gene control of Leber hereditary optic neuropathy: evidence from segregation analysis for dependence on X chromosome inactivation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Evidence for a Novel X-Linked Modifier Locus for Leber Hereditary Optic Neuropathy

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Identification of an X-chromosomal locus and haplotype modulating the phenotype of a mitochondrial DNA disorder

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of leber hereditary optic neuropathy in Chinese families with the m.11778G-->a mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation

1 reference

https://api.crossref.org/works/10.1016/J.YMGME.2010.07.014

7 January 2021

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10.1016/J.YMGME.2010.07.014

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Europe PubMed Central

PubMed publication ID

11 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

11 November 2017

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