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Invertebrate Models of Kallmann Syndrome: Molecular Pathogenesis and New Disease Genes
Kallmann Syndrome is a heritable disorder characterized by congenital anosmia, hypogonadotropic hypogonadism and, less frequently, by other symptoms. The X-linked form of this syndrome is caused by mutations affecting the KAL1 gene that codes for the extracellular protein anosmin-1. Investigation of...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Bentham Science Publishers
2013
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3580776/ https://www.ncbi.nlm.nih.gov/pubmed/23997646 http://dx.doi.org/10.2174/138920213804999174 |