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GENATLAS PHENOTYPE |
last update : 08-10-2013 |
Symbol | SPG19 |
Location | 9q33-q34 |
HGNC id | 16706 |
Name | spastic paraplegia 19 |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | neurology |
Type | disease |
Remark(s) |