Refinement of the PARK3 locus on chromosome 2p13 and the analysis of 14 candidate genes.

Published

Journal Article

Parkinson's disease (PD) is a common neurodegenerative disorder with clinical features of bradykinesia, rigidity, resting tremor and postural instability resulting from the deficiency of dopamine in the nigrostriatal system. Previously we mapped a susceptibility gene for an autosomal dominant form of PD to a 10.6 cM region of chromosome 2p (PARK3; OMIM 602404). A common haplotype shared by two North American kindreds (Families B and C) genealogically traced to Southern Denmark and Northern Germany suggested a founder effect. Here we report progress in the refinement of the PARK3 locus and sequence analysis of candidate genes within the region. Members of families B and C were genotyped using polymorphic markers, reducing the minimum common haplotype to eight markers spanning a physical distance of 2.5 Mb. Analysis of 14 genes within the region did not reveal any potentially pathogenic mutations segregating with the disease, implying that none of these genes are likely candidates for PARK3.

Full Text

Duke Authors

Cited Authors

  • West, AB; Zimprich, A; Lockhart, PJ; Farrer, M; Singleton, A; Holtom, B; Lincoln, S; Hofer, A; Hill, L; Müller-Myhsok, B; Wszolek, ZK; Hardy, J; Gasser, T

Published Date

  • September 2001

Published In

Volume / Issue

  • 9 / 9

Start / End Page

  • 659 - 666

PubMed ID

  • 11571553

Pubmed Central ID

  • 11571553

International Standard Serial Number (ISSN)

  • 1018-4813

Digital Object Identifier (DOI)

  • 10.1038/sj.ejhg.5200698

Language

  • eng

Conference Location

  • England