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

Novel mitochondrial DNA mutations in Parkinson's disease.

Journal of neural transmission (Vienna, Austria : 1996) - 1 May 2002

Richter G, Sonnenschein A, Grünewald T, Reichmann H, Janetzky B

Abstract excerpt

Despite the recent discovery of several chromosomal gene mutations in familial Parkinson's disease (PD) the genetic background for idiopathic PD remains to be elusive. Since the discovery of 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP) action on dopaminergic neuronal cells and the specific...

Read the complete abstract on PubMed

Topics

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

Share to Blood Platelets
Share to DNA, Mitochondrial
Share to Electron Transport Complex I

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to NADH Dehydrogenase

Share to NADH, NADPH Oxidoreductases

Share to Parkinson Disease

Share to Reference Values

Share to Substantia Nigra

Source

Identifiers

PMID: 12111463
DOI: 10.1007/s007020200060

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-12111463-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Novel mitochondrial DNA mutations in Parkinson's disease.PMID 12111463Read ↗

Damage in Mitochondrial DNA Associated with Parkinson's DiseaseSemantic proximity Read ↗

Sequence analysis of the entire mitochondrial genome in Parkinson's disease.Semantic proximity Read ↗

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

Parkinson's disease and mitochondrial gene variations: a review.Semantic proximity Read ↗

Mitochondrial DNA in Parkinson's disease.Semantic proximity Read ↗

Mitochondrial DNA analysis in Parkinson's diseaseSemantic proximity Read ↗

[Mitochondrial DNA and Parkinson disease. Methodologic review].Semantic proximity Read ↗

Somatic mtDNA variation is an important component of Parkinson's diseaseSemantic proximity Read ↗

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

Reduced mitochondrial DNA copy number is a biomarker of Parkinson's diseaseSemantic proximity Read ↗

A blood-based marker of mitochondrial DNA damage in Parkinson’s diseaseSemantic proximity Read ↗

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

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