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Article

Association of codon 167 Ser/Asn heterozygosity in the parkin gene with sporadic Parkinson's disease.

Neuroreport - 9 Sept 1999

Satoh J, Kuroda Y

Abstract excerpt

A variety of deletional and point mutations has been identified in the parkin gene on chromosome 6q25.2-27 in patients with autosomal recessive juvenile parkinsonism, a distinct form of familial Parkinson's disease (PD). To study the potential involvement of the parkin gene in development of non-hereditary idiopathic PD, a codon 167 serine/asparagine (167S/N) polymorphism located in its exon 4 was analyzed by...

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Identifiers

PMID: 10511432
DOI: 10.1097/00001756-199909090-00008

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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.

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Association of codon 167 Ser/Asn heterozygosity in the parkin gene with sporadic Parkinson's disease.PMID 10511432Read ↗

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Coding polymorphisms in the parkin gene and susceptibility to Parkinson disease.Semantic proximity Read ↗

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Heterozygous parkin point mutations are as common in control subjects as in Parkinson's patients.Semantic proximity Read ↗

PARKIN-coding polymorphisms are not associated with Parkinson's disease in a population from northeastern Mexico.Semantic proximity Read ↗

Frequency of heterozygous Parkin mutations in healthy subjects: need for careful prospective follow-up examination of mutation carriers.Semantic proximity Read ↗

Polymorphisms of the parkin gene in sporadic Parkinson's disease among Chinese in Taiwan.Semantic proximity Read ↗

Influence of heterozygosity for parkin mutation on onset age in familial Parkinson disease: the GenePD study.Semantic proximity Read ↗

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