Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome by Kim Hyung-Goo, Kurth Ingo, Lan Fei, Meliciani Irene, Wenzel Wolfgang, Eom Soo Hyun, Kang Gil Bu, Rosenberger Georg, Tekin Mustafa, Ozata Metin, Bick David P, Sherins Richard J, Walker Steven L, Shi Yang, Gusella James F, Layman Lawrence C in American journal of human genetics (2008).

[PMID: 18834967] PubMed

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