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The identification of HESX1 mutations in Kallmann syndrome
OBJECTIVE: To determine if HESX1 mutations are present in patients with idiopathic hypogonadotropic hypogonadism (IHH)/Kallmann syndrome (KS). HESX1 mutations have previously been characterized in patients with septo-optic dysplasia (SOD), isolated growth hormone deficiency (IGHD), and combined pitu...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3888813/ https://ncbi.nlm.nih.gov/pubmed/23465708 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.fertnstert.2013.01.149 |
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