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Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
scientific article
Author/s
author: Ingo Kurth, Mustafa Tekin, Wolfgang Wenzel, James F. Gusella, Irene Meliciani, Richard J Sherins
Work details
Publication date
October 2008
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Language
English
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