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Q24657612-38E0F499-8CF2-4B97-AE9C-E20415D9381C
Q24657612-38E0F499-8CF2-4B97-AE9C-E20415D9381C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24657612-38E0F499-8CF2-4B97-AE9C-E20415D9381C
Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
P2860
Q24657612-38E0F499-8CF2-4B97-AE9C-E20415D9381C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24657612-38E0F499-8CF2-4B97-AE9C-E20415D9381C
rank
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Statement
wasDerivedFrom
714113170332770f2b8b29d14ef4b43b76a3bcb2
P2860
Phenotypic spectrum of CHARGE syndrome in fetuses with CHD7 truncating mutations correlates with expression during human development.