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References | OMIM | Gene | GeneReviews | HGMD | HGNC |
GENATLAS PHENOTYPE |
last update : 08-06-2022 |
Symbol | SPGF66 |
Location | 7p12.2 |
Name | spermatogenic failure 66 |
Corresponding gene | ZPBP |
Main clinical features |
|
Genetic determination | autosomal recessive |
Function/system disorder | sex-genitalia |
Type | disease |
Remark(s) |