Mutations in fibroblast growth factor receptor 1 cause both Kallmann syndrome and normosmic idiopathic hypogonadotropic hypogonadism.

Source:http://linkedlifedata.com/resource/pubmed/id/16606836

Proc. Natl. Acad. Sci. U.S.A. 2006 Apr 18 103 16 6281-6

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PMID
16606836