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SAT-287 Hypogonadotropic Hypogonadism in RPL10 Mutation-Associated Syndromic Intellectual Disability
Background: A multitude of inactivating genetic mutations have been implicated in Idiopathic Hypogonadotropic Hypogonadism (IHH), either in Kallmann syndrome or in norm-osmic IHH. Over the last decade, a limited number of studies described variations in ribosomal protein L10 (RPL10) gene as a cause...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
| Publicado: |
Endocrine Society
2019
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6552257/ http://dx.doi.org/10.1210/js.2019-SAT-287 |