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Q49437047-24480817-FCD2-49EF-A2F0-58D5978670D1
Q49437047-24480817-FCD2-49EF-A2F0-58D5978670D1
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http://www.wikidata.org/entity/statement/Q49437047-24480817-FCD2-49EF-A2F0-58D5978670D1
Update on the Genetics of Idiopathic Hypogonadotropic Hypogonadism.
P2860
Q49437047-24480817-FCD2-49EF-A2F0-58D5978670D1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q49437047-24480817-FCD2-49EF-A2F0-58D5978670D1
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wasDerivedFrom
7a4394cb6198ae8c170781d8ce59d0f09e9a1ecb
P2860
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome