| Literature DB >> 15541303 |
Jie Shen1.
Abstract
Two papers in this issue of Neuron identify a causative gene, LRRK2, for familial parkinsonism. Several dominantly inherited missense mutations have been identified in a number of families that exhibit a broad spectrum of neuropathological features, including deposition of alpha-synuclein and tau proteins. The LRRK2 gene is predicted to encode a large protein containing leucine-rich repeats and Ras/GTPase, tyrosine kinase-like, and WD40 domains.Entities:
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Year: 2004 PMID: 15541303 DOI: 10.1016/j.neuron.2004.11.008
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173