Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.

Parkinsonism & related disorders - 1 Dec 2010

Nishioka Kenya, Vilariño-Güell Carles, Cobb Stephanie A, Kachergus Jennifer M, Ross Owen A, Hentati Emna, Hentati Faycal, Farrer Matthew J

Abstract excerpt

NADH dehydrogenase ubiquinone flavoprotein 2 (NDUFV2), encoding a subunit of mitochondrial complex I, is a candidate gene for several neuronal diseases; schizophrenia, bipolar disorder and Parkinson disease (PD). We screened the entire coding region of NDUFV2 in 33 familial PD patients of North African Arab-Berber ethnicity in which all known genetic forms of PD had been excluded. We detected one novel...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Africa, Northern
Share to Age of Onset

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Amino Acid Substitution

Share to Electron Transport Complex I

Share to Heterozygote

Share to NADH Dehydrogenase

Share to Parkinson Disease

Share to Reverse Transcriptase Polymerase Chain Reaction

Source

Open in PubMed Open full text

Identifiers

PMID: 20971673
DOI: 10.1016/j.parkreldis.2010.09.007
PMCID: PMC4381965

Genes

NDUFV2

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variation of the mitochondrial complex I subunit NDUFV2 and Parkinson's disease.PMID 20971673Read ↗

Comprehensive sequencing of the LRRK2 gene in patients with familial Parkinson's disease from North Africa.Semantic proximity Read ↗

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

An analysis of genetic studies of Parkinson's disease in Africa.Semantic proximity Read ↗

Leucine rich repeat kinase 2 (LRRK2) gly2019ser mutation is absent in a second cohort of nigerian africans with parkinson diseaseSemantic proximity Read ↗

LRRK2 G2019S in the North African population: a review.Semantic proximity Read ↗

Leucine rich repeat kinase 2 (LRRK2) GLY2019SER mutation is absent in a second cohort of Nigerian Africans with Parkinson diseaseSemantic proximity Read ↗

Mitochondrial polymorphisms significantly reduce the risk of Parkinson disease.Semantic proximity Read ↗

Novel mutations of mitochondrial complex I in pathologically proven Parkinson disease.Semantic proximity Read ↗

Mutations in the complex I NDUFS2 gene of patients with cardiomyopathy and encephalomyopathy.Semantic proximity Read ↗

Association study on the mitochondrial gene NDUFV2 and bipolar disorder in the Chinese Han population.Semantic proximity Read ↗

Association of mitochondrial complex I subunit gene NDUFV2 at 18p11 with schizophrenia in the Japanese population.Semantic proximity Read ↗

A haplotype in the 5'-upstream region of the NDUFV2 gene is associated with major depressive disorder in Han Chinese.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.