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Q34752030-65411803-6DDD-4355-B30B-DE3A7AEFC30D
Q34752030-65411803-6DDD-4355-B30B-DE3A7AEFC30D
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http://www.wikidata.org/entity/statement/Q34752030-65411803-6DDD-4355-B30B-DE3A7AEFC30D
Functionally compromised CHD7 alleles in patients with isolated GnRH deficiency.
P2860
Q34752030-65411803-6DDD-4355-B30B-DE3A7AEFC30D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34752030-65411803-6DDD-4355-B30B-DE3A7AEFC30D
rank
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type
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wasDerivedFrom
5657c9c46b9b4fe1534110fda2f0e861a9f400c8
P2860
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome