Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndrome (Q73729902)

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6 November 2019

title

Analysis of the mitochondrial DNA from patients with Wolfram (DIDMOAD) syndrome (English)

1 reference

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6 November 2019

author name string

S. Hofmann

1

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17 November 2024

R. Bezold

2

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17 November 2024

M. Jaksch

3

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17 November 2024

P. Kaufhold

4

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17 November 2024

B. Obermaier-Kusser

5

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17 November 2024

K. D. Gerbitz

6

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17 November 2024

language of work or name

English

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National Center for Biotechnology Information

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17 November 2024

publication date

1 September 1997

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6 November 2019

September 1997

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National Center for Biotechnology Information

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Molecular and Cellular Biochemistry

17 November 2024

published in

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6 November 2019

volume

174

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6 November 2019

issue

1-2

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6 November 2019

page(s)

209-213

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Sequence and organization of the human mitochondrial genome

6 November 2019

cites work

1 reference

12 December 2020

mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region

1 reference

12 December 2020

Mitochondrial genetics: a paradigm for aging and degenerative diseases?

1 reference

12 December 2020

Autosomal recessive Wolfram syndrome associated with an 8.5-kb mtDNA single deletion

1 reference

12 December 2020

Linkage of the gene for Wolfram syndrome to markers on the short arm of chromosome 4

1 reference

12 December 2020

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

12 December 2020

Phylogenetic analysis of the mitochondrial genomes from Leber hereditary optic neuropathy pedigrees

1 reference

12 December 2020

Wolfram syndrome: a mitochondrial-mediated disorder?

1 reference

12 December 2020

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

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

12 December 2020

Features of mtDNA mutation patterns in European pedigrees and sporadic cases with Leber hereditary optic neuropathy.

1 reference

12 December 2020

Mutations in mitochondrial tRNA genes: non-linkage with syndromes of Wolfram and chronic progressive external ophthalmoplegia

1 reference

12 December 2020

Diseases of the mitochondrial DNA.

1 reference

12 December 2020

Neurodegeneration and diabetes: UK nationwide study of Wolfram (DIDMOAD) syndrome.

1 reference

12 December 2020

Diabetes mellitus associated with a pathogenic point mutation in mitochondrial DNA

1 reference

12 December 2020

Mitochondrial mutation commonly associated with Leber's hereditary optic neuropathy observed in a patient with Wolfram syndrome (DIDMOAD)

1 reference

12 December 2020

Deletion of mitochondrial DNA in a case of early-onset diabetes mellitus, optic atrophy, and deafness (Wolfram syndrome, MIM 222300).

1 reference

12 December 2020

MtDNA mutations associated with Leber's hereditary optic neuropathy: studies on cytoplasmic hybrid (cybrid) cells.

1 reference

12 December 2020

Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness

1 reference

12 December 2020