Title : A common leucine-rich repeat kinase 2 gene mutation in familial and sporadic Parkinson's disease in Russia.

Pub. Date : 2007 Apr

PMID : 17388990






2 Functional Relationships(s)
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1 All patients carrying the LRRK2 G2019S exhibited typical levodopa-responsive parkinsonism, and severe levodopa-induced dyskinesia was observed in the patient carrying the LRRK2 and parkin mutations. Levodopa leucine rich repeat kinase 2 Homo sapiens
2 All patients carrying the LRRK2 G2019S exhibited typical levodopa-responsive parkinsonism, and severe levodopa-induced dyskinesia was observed in the patient carrying the LRRK2 and parkin mutations. Levodopa leucine rich repeat kinase 2 Homo sapiens