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

Analysis of the PINK1 Gene in a Large Cohort of Cases With Parkinson Disease

1 Dec 2004

Abstract excerpt

BACKGROUND: Mutations in the PTEN-induced kinase (PINK1) gene located within the PARK6 locus on chromosome 1p35-p36 have recently been identified in patients with recessive early-onset Parkinson disease. OBJECTIVE: To assess the prevalence of PINK1 mutations within a series of early- and late-onset Parkinson disease patients living in North America. DESIGN: All coding exons of the PINK1 gene were sequenced in a...

Read the complete abstract on PubMed

Topics

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

Share to Nuclear Receptors and Signaling
Share to Parkinson's Disease and Spinal Disorders
Share to Parkinson's Disease Mechanisms and Treatments

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

Source

Identifiers

PMID: 15596610
DOI: 10.1001/archneur.61.12.1898

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.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of the PINK1 Gene in a Large Cohort of Cases With Parkinson DiseasePMID 15596610Read ↗

Mutational analysis of the PINK1 gene in early-onset parkinsonism in Europe and North Africa.Semantic proximity Read ↗

Novel PINK1 mutations in early-onset parkinsonism.Semantic proximity Read ↗

Mutation analysis of PINK1 gene in patients with early-onset Parkinsonism.Semantic proximity Read ↗

Parkin and PINK1 mutations in early-onset Parkinson's disease: comprehensive screening in publicly available cases and control.Semantic proximity Read ↗

Comprehensive assessment of <i>PINK1</i> variants in Parkinson’s diseaseSemantic proximity Read ↗

Comprehensive assessment of PINK1 variants in Parkinson's disease.Semantic proximity Read ↗

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism.Semantic proximity Read ↗

Genetic analysis of PARK2 and PINK1 genes in Brazilian patients with early-onset Parkinson's disease.Semantic proximity Read ↗

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.Semantic proximity Read ↗

PINK1 mutations in a Brazilian cohort of early-onset Parkinson's disease patients.Semantic proximity Read ↗

PINK1 mutations in sporadic early-onset Parkinson's disease.Semantic proximity Read ↗

A common A340T variant in PINK1 gene associated with late-onset Parkinson's disease in Chinese.Semantic proximity Read ↗

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