Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease (Q35240670)

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14 January 2020

title

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease (English)

1 reference

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14 January 2020

1 reference

1 reference

Carles Vilariño-Güell

2

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14 January 2020

Matthew J. Farrer

8

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14 January 2020

4

Jennifer M Kachergus

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14 January 2020

author name string

Kenya Nishioka

1

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14 January 2020

Stephanie A Cobb

3

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14 January 2020

Emna Hentati

6

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14 January 2020

Faycal Hentati

7

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14 January 2020

Owen A Ross

5

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14 January 2020

language of work or name

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23 October 2010

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Parkinsonism and Related Disorders

14 January 2020

number of pages

2

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based on heuristic

inferred from page(s)

published in

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14 January 2020

volume

16

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14 January 2020

issue

10

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14 January 2020

page(s)

686-687

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A comparative study of LRRK2, PINK1 and genetically undefined familial Parkinson's disease

14 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Mitochondrial biology and oxidative stress in Parkinson disease pathogenesis

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

PINK1 mutations and parkinsonism

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

LRRK2 Gly2019Ser penetrance in Arab-Berber patients from Tunisia: a case-control genetic study

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Screening for Lrrk2 G2019S and clinical comparison of Tunisian and North American Caucasian Parkinson's disease families

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Complex I polymorphisms, bigenomic heterogeneity, and family history in Virginians with Parkinson's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Genetics of Parkinson disease: paradigm shifts and future prospects.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with bipolar disorder.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Mutation in the alpha-synuclein gene identified in families with Parkinson's disease

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

What features improve the accuracy of clinical diagnosis in Parkinson's disease: A clinicopathologic study

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

Calbindin 1, fibroblast growth factor 20, and alpha-synuclein in sporadic Parkinson's disease.

27 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4381965

10.1016/J.PARKRELDIS.2010.09.007

26 September 2018

Identifiers

DOI

1 reference

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14 January 2020

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14 January 2020

PubMed publication ID

20971673

1 reference