The CFTR polymorphisms poly-T, TG-repeats and M470V in Chinese males with congenital bilateral absence of the vas deferens

Congenital bilateral absence of the vas deferens (CBAVD) is a frequent cause of obstructive azoospermia, and mutations of the cystic fibrosis transmembrane conductance regulator (CFTR) gene have also been frequently identified in patients with CBAVD. However, the distribution of the CFTR polymorphis...

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Main Authors: Ni, Wu-Hua, Jiang, Lei, Fei, Qian-Jin, Jin, Jian-Yuan, Yang, Xu, Huang, Xue-Feng
Formato: Artigo
Idioma:Inglês
Publicado em: Nature Publishing Group 2012
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Original Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3734982/
https://ncbi.nlm.nih.gov/pubmed/22842702
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/aja.2012.43
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