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GENATLAS PHENOTYPE |
last update : 12-11-2020 |
Symbol | ETM4 |
Location | 16p11.2 |
Name | essential tremor, hereditary, 4 |
Corresponding gene | FUS |
Main clinical features |
|
Genetic determination | autosomal dominant |
Function/system disorder | neurology |
Type | disease |
Mechanism(s) |
Gene mutation | Chromosome rearrangement | Effect | Comments |
| various types
|  
| abnormal protein/loss of function
|  
| |
Remark(s) |