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[CHD7 represents the first identified chromatin-remodeling protein with a role in human puberty and the second gene to cause both normosmic idiopathic hypogonadotropic hypogonadism and Kallmann syndrome in humans]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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Gene-disease associations inferred from text-mining the literature.
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