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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 05-09-2012 |
Symbol | PARK17 |
Location | 16q11.2 |
Name | Parkinson disease 17 |
Corresponding gene | VPS35 |
Main clinical features |
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Genetic determination | autosomal dominant |
Function/system disorder | neurology |
Type | disease |
Remark(s) |