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Genetic Polymorphism in the RYR1 C6487T Is Associated with Severity of Hypospadias in Chinese Han Children

OBJECTIVE: Hypospadias is a common congenital malformation of the male external genitalia. Most cases have an unknown etiology, which is probably a mix of monogenic and multifactorial forms, implicating both genetic and environmental factors. Ryanodine receptor 1 (RYR1) mutations are a common cause...

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Detalles Bibliográficos
Autores principales:	Zhang, Haiyan, Zhang, Zhuo, Jia, Linpei, Ji, Wei, Li, Hai
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi 2018
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6031201/ https://www.ncbi.nlm.nih.gov/pubmed/30027098 http://dx.doi.org/10.1155/2018/7397839

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