CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family

CFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family

Cystic fibrosis (CF) is one of the most common recessive genetic diseases, with a wide spectrum of phenotypes, ranging from infertility to severe pulmonary disease. Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are considered the main genetic cause for CF. In this...

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Bibliographic Details
Main Authors: Mahdieh Daliri Ghouchanatigh, Ranjha Khan, Majid Mojarrad, Uzma Hameed, Muhammad Zubair, Ahmed Waqas, Mohsen Jalali, Mahmoudreza Kalantari, Ali Shamsa, Huan Zhang, Qing-Hua Shi
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2022-01-01
Series:Asian Journal of Andrology
Subjects:
congenital absence of the uterus; congenital unilateral absence of the vas deferens; cystic fibrosis transmembrane conductance regulator; whole-exome sequencing
Online Access:http://www.ajandrology.com/article.asp?issn=1008-682X;year=2022;volume=24;issue=4;spage=416;epage=421;aulast=

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http://www.ajandrology.com/article.asp?issn=1008-682X;year=2022;volume=24;issue=4;spage=416;epage=421;aulast=

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