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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 25-02-2009 |
Symbol | LQT9 |
Location | 3p25 |
Name | long QT syndrome 9 |
Corresponding gene | CAV3 |
Main clinical features |
|
Genetic determination | not applicable |
Related entries | . sudden infant death syndrome |
Function/system disorder | cardiovascular |
Type | disease |
Mechanism(s) |
Gene mutation | Chromosome rearrangement | Effect | Comments | |
---|---|---|---|---|
various types | abnormal protein/gain of function |
Remark(s) |