An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain (Q61647463)
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Language | Label | Description | Also known as |
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English | An Uncommon Phenotype with Familial Central Hypogonadism Caused by a NovelPROP1Gene Mutant Truncated in the Transactivation Domain |
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Statements
An uncommon phenotype with familial central hypogonadism caused by a novel PROP1 gene mutant truncated in the transactivation domain (English)
Rachel Reynaud
Sophie Vallette-Kasic
Marie-Pierre Guillet
Gilbert Simonin
Alain Enjalbert