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...

Descripción completa

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

Internet

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

Ejemplares similares