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Article

Genealogical studies in LRRK2-associated Parkinson's disease in central Norway.

Parkinsonism & related disorders - 1 Sept 2010

Johansen Krisztina K, Hasselberg Kåre, White Linda R, Farrer Matthew J, Aasly Jan O

Abstract excerpt

The most common mutation related to Parkinson's disease (PD) is the p.G2019S mutation in the LRRK2 gene. Global population frequencies and crude estimates of haplotype conservation suggest most carriers are related. A total of 671 Norwegian PD patients and 215 of their family members were screened for the LRRK2 p.G2019S mutation. Twenty-one PD cases and 44 family members were positive for the mutation and all...

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Identifiers

PMID: 20621541
DOI: 10.1016/j.parkreldis.2010.05.005

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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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