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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Detalles Bibliográficos
Autores principales: Wang, Ya-Yun, Lin, Ying-Hung, Wu, Yi-No, Chen, Yen-Lin, Lin, Yung-Chih, Cheng, Chiao-Yin, Chiang, Han-Sun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398719/
https://www.ncbi.nlm.nih.gov/pubmed/28384194
http://dx.doi.org/10.1371/journal.pgen.1006715

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5398719/
https://www.ncbi.nlm.nih.gov/pubmed/28384194
http://dx.doi.org/10.1371/journal.pgen.1006715

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