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

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

Genomics - 1 Apr 1998

Hattori N, Yoshino H, Tanaka M, Suzuki H, Mizuno Y

Abstract excerpt

We analyzed the gene encoding the 24-kDa subunit of mitochondrial complex I, which has been implicated in the pathogenesis of Parkinson disease (PD). We set out to identify a polymorphism in the 24-kDa subunit gene (NDUFV2) in patients with PD and determine whether genetic polymorphism of this ge...

Read the complete abstract on PubMed

Topics

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

Share to Amino Acid Sequence
Share to Cattle
Share to Disease Susceptibility

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Genotype

Share to Mitochondria

Share to Molecular Sequence Data

Share to Sequence Homology, Amino Acid

Source

Identifiers

PMID: 9570948
DOI: 10.1006/geno.1997.5192

Genes

NDUFV2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 1 Sept 2026. Prepared record publication-9570948-2026-09-01.1. Manifest publication-graph-cohort-2026-09-01.1.

Source receipt: PubMed via Helena Literature Corpus, retrieved 1 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease.PMID 9570948Read ↗

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

A polymorphism located at an ATG transcription start site of the heme oxygenase-2 gene is associated with classical Parkinson's disease.Semantic proximity Read ↗

Complex I polymorphisms, bigenomic heterogeneity, and family history in Virginians with Parkinson's disease.Semantic proximity Read ↗

Analysis of vesicular monoamine transporter 2 polymorphisms in Parkinson's disease.Semantic proximity Read ↗

Parkinson disease: analysis of mitochondrial DNA in monozygotic twins.Semantic proximity Read ↗

Mitochondrial ND1 sequence analysis and association of the T4216C mutation with Parkinson's disease.Semantic proximity Read ↗

The dopamine D2 receptor gene is a susceptibility locus for Parkinson's disease.Semantic proximity Read ↗

A novel screen for nuclear mitochondrial gene associations with Parkinson's disease.Semantic proximity Read ↗

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

Mitochondrial NADH dehydrogenase and CYP2D6 genotypes in Lewy-body parkinsonism.Semantic proximity Read ↗

Variability and validity of polymorphism association studies in Parkinson's disease.Semantic proximity Read ↗

An association study between Heme oxygenase-1 genetic variants and Parkinson's diseaseSemantic proximity Read ↗

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