Title : The discovery of LRRK2 p.R1441S, a novel mutation for Parkinson's disease, adds to the complexity of a mutational hotspot.

Pub. Date : 2016 Oct

PMID : 27111571






1 Functional Relationships(s)
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1 The clinical characteristics of affected family members were similar to those described in PD families with other mutations in LRRK2 codon 1441 and included resting tremor, rigidity, bradykinesia, unilateral onset, and a good response to levodopa. Levodopa leucine rich repeat kinase 2 Homo sapiens