Title : Autosomal recessive parkinsonism.

Pub. Date : 2012 Jan

PMID : 22166450






2 Functional Relationships(s)
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Compound Name
Protein Name
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1 In three forms, caused by mutations in parkin (PARK2), PINK1 (PARK6), or DJ-1 (PARK7), the phenotype is usually characterized by levodopa-responsive parkinsonism without atypical features. Levodopa PTEN induced kinase 1 Homo sapiens
2 In three forms, caused by mutations in parkin (PARK2), PINK1 (PARK6), or DJ-1 (PARK7), the phenotype is usually characterized by levodopa-responsive parkinsonism without atypical features. Levodopa PTEN induced kinase 1 Homo sapiens