Loss of SLC9A3 decreases CFTR protein and causes obstructed azoospermia in mice

Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene cause cystic fibrosis (CF) and are associated with congenital bilateral absence of the vas deferens (CBAVD), which is the major cause of infertility in male patients with CF. However, most Taiwanese patients with CBAVD...

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Detalhes bibliográficos
Publicado no:PLoS Genet
Main Authors: Wang, Ya-Yun, Lin, Ying-Hung, Wu, Yi-No, Chen, Yen-Lin, Lin, Yung-Chih, Cheng, Chiao-Yin, Chiang, Han-Sun
Formato: Artigo
Idioma:Inglês
Publicado em: Public Library of Science 2017
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC5398719/
https://ncbi.nlm.nih.gov/pubmed/28384194
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pgen.1006715
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