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Whole exome sequencing identifies deleterious rare variants in CCDC141 in familial self-limited delayed puberty
Developmental abnormalities of the gonadotropin-releasing hormone (GnRH) neuronal network result in a range of conditions from idiopathic hypogonadotropic hypogonadism to self-limited delayed puberty. We aimed to discover important underlying regulators of self-limited delayed puberty through interr...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8688425/ https://www.ncbi.nlm.nih.gov/pubmed/34930920 http://dx.doi.org/10.1038/s41525-021-00274-w |