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Q21131272-16D74B31-F1A7-4716-BBF4-F3494FCD9EBC
Q21131272-16D74B31-F1A7-4716-BBF4-F3494FCD9EBC
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Statement
http://www.wikidata.org/entity/statement/Q21131272-16D74B31-F1A7-4716-BBF4-F3494FCD9EBC
Reproduction, smell, and neurodevelopmental disorders: genetic defects in different hypogonadotropic hypogonadal syndromes
P2860
Q21131272-16D74B31-F1A7-4716-BBF4-F3494FCD9EBC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21131272-16D74B31-F1A7-4716-BBF4-F3494FCD9EBC
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wasDerivedFrom
8928dbbfd0dcf6c4b1c892c5766a0e00240d5b89
P2860
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome