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| | Parkinson's disease - Wikipedia, the free encyclopedia |
 | | PARK3 (OMIM %602404), mapped to 2p, autosomal dominant, only described in a few kindreds. |
 | | PARK5, caused by mutations in the UCHL1 gene (OMIM +191342) which codes for the protein ubiquitin carboxy-terminal hydrolase L1 |
 | | PARK6 (OMIM #605909), caused by mutations in PINK1 (OMIM *608309) which codes for the protein PTEN-induced putative kinase 1. |
| en.wikipedia.org /wiki/Parkinson%27s_disease (6881 words) |
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