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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...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Ni, Wu-Hua, Jiang, Lei, Fei, Qian-Jin, Jin, Jian-Yuan, Yang, Xu, Huang, Xue-Feng
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: Nature Publishing Group 2012
विषय:
ऑनलाइन पहुंच: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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