Neurology. 2005 Sep 13;65(5):741-4.

A clinic-based study of the LRRK2 gene in Parkinson disease yields new mutations.

Zabetian CP, Samii A, Mosley AD, Roberts JW, Leis BC, Yearout D, Raskind WH, Griffith A.

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Department of Neurology, University of Washington School of Medicine, Seattle, WA, USA. zabetian@u.washington.edu

Abstract

Referral-based studies indicate that a mutation (G2019S) in exon 41 of the LRRK2 gene might be a common cause of Parkinson disease (PD). The authors sequenced leucine-rich repeat kinase 2 (LRRK2) exons 31, 35, and 41 in 371 consecutively recruited patients with PD and found mutations in six (1.6%) subjects, including two heterozygous for new putative pathogenic variants (R1441H, IVS31 + 3A-->G). These data confirm the important contribution of LRRK2 to PD susceptibility in a clinic-based population.

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LRRK2: both a cause and a risk factor for Parkinson disease? [Neurology. 2005]
LRRK2: both a cause and a risk factor for Parkinson disease?Foroud T. Neurology. 2005 Sep 13; 65(5):664-5.

PMID:: 16157909; [PubMed - indexed for MEDLINE]

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Neurology. 2005 Sep 13 ;65(5):741-4.

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