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Molecular Basis for the Kallmann Syndrome-Linked Fibroblast Growth Factor Receptor Mutation
Kallmann syndrome (KS) is a developmental disease that expresses in patients as hypogonadotropic hypogonadism and anosmia. KS is commonly associated with mutations in the extracellular D2 domain of the fibroblast growth factor receptor (FGFR). In this study, for the first time, the molecular basis f...
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| Autores principales: | , , , |
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| Formato: | Artigo |
| Lenguaje: | Inglês |
| Publicado: |
2012
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| Materias: | |
| Acceso en línea: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3729937/ https://ncbi.nlm.nih.gov/pubmed/22842457 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.bbrc.2012.07.104 |
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