CFTR variants and renal abnormalities in males with congenital unilateral absence of the vas deferens (CUAVD): a systematic review and meta-analysis of observational studies

PURPOSE: CFTR variant is the main genetic contributor to congenital (unilateral/bilateral) absence of the vas deferens (CAVD/CUAVD/CBAVD). We performed a systematic review to elucidate the genetic link between CFTR variants, CUAVD, and the associated risk of renal abnormality (RA). METHODS: We searc...

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Detalles Bibliográficos
Autores principales: Cai, Hongcai, Qing, Xingrong, Niringiyumukiza, Jean Damascene, Zhan, Xuxin, Mo, Dunsheng, Zhou, Yuanzhong, Shang, Xuejun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group US 2018
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752674/
https://www.ncbi.nlm.nih.gov/pubmed/30214069
http://dx.doi.org/10.1038/s41436-018-0262-7

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6752674/
https://www.ncbi.nlm.nih.gov/pubmed/30214069
http://dx.doi.org/10.1038/s41436-018-0262-7

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