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Article

Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from northern Germany.

Annals of human genetics - 1 Jul 1999

Klein C, Vieregge P, Hagenah J, Sieberer M, Doyle E, Jacobs H, Gasser T, Breakefield X O, Risch N J, Ozelius L J

Abstract excerpt

A founder haplotype on chromosome 2p for autosomal dominant Parkinson's disease (PD) has been postulated for two families of Northern European descent, and a new mutation in the alpha-synuclein gene (Ala30Pro) has been found in a German PD family. We evaluated 85 German PD patients and 85 ethnica...

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Source

Identifiers

PMID: 10738540
DOI: 10.1046/j.1469-1809.1999.6340285.x

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 4 Sept 2026. Prepared record publication-10738540-2026-09-04.2. Manifest publication-graph-cohort-2026-09-04.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 4 Sept 2026.

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