期刊
MOVEMENT DISORDERS
卷 20, 期 12, 页码 1653-1655出版社
WILEY
DOI: 10.1002/mds.20682
关键词
LRRK2; dardarin; PARK8; Parkinson's disease
LRRK2 mutations have recently been described in families with Parkinson's disease. Here we show that one of them (G2019S) is present in 6% (7 of 124) unrelated cases of disease in a clinic-based sample series from central Portugal, but not present in 126 controls from the same population. Thus, LRRK2 mutations appear to be a common cause of typical Parkinson's disease and as such will alter clinical practice. (c) 2005 Movement Disorder Society.
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