Loss-of-function mutation in the prokineticin 2 gene causes Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.

Source:http://linkedlifedata.com/resource/pubmed/id/17959774

Proc. Natl. Acad. Sci. U.S.A. 2007 Oct 30 104 44 17447-52

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PMID
17959774