Mutations in CHD7, encoding a chromatin-remodeling protein, cause idiopathic hypogonadotropic hypogonadism and Kallmann syndrome
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| Description | scientific article |
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author: Ingo Kurth Irene Meliciani Richard J Sherins James F. Gusella Wolfgang Wenzel Mustafa Tekin |
| Publication date | October 2008 |
| Language | English |
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| Missing/wrong data? | Edit Wikidata item |