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• (author = "Martinez, D.")
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Molecular pathogenesis of Kallmann's syndrome.

Author(s) : Cadman, SM , Kim, SH , Hu, Y , González-Martínez, D , Bouloux, PM
Description : Hypogonadotrophic hypogonadism (HH) is characterized by delayed or absent pubertal development secondary to gonadotrophin deficiency. HH can result from mutations of the gonadotrophin-releasing hormone receptor 1, the gonadotrophin beta-subunits, or various transcription factors involved in pituitar...
Repository : UCL Eprints , View repository documents
Language(s) : English
Subject(s) : Extracellular Matrix Proteins, Genes, Dominant, Genes, X-Linked, Gonadotropin-Releasing Hormone, Heparan Sulfate Proteoglycans, Humans, Kallmann Syndrome, Models, Biological, Nerve Tissue Proteins, Olfactory Bulb, Receptor, Fibroblast Growth Factor, Type 1, Receptors, LHRH, Signal Transduction
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Publication Date(s) : 2007-01-01