Open AccessCFTR mutations causing congenital unilateral absence of the vas deferens (CUAVD) and congenital absence of the uterus (CAU) in a consanguineous family
Author(s) -
Mahdieh Daliri Ghouchanatigh,
Ranjha Khan,
Majid Mojarrad,
Uzma Hameed,
Muhammad Zubair,
Ahmed Waqas,
Mohsen Jalali,
Mahmoud Reza Kalantari,
Ali Shamsa,
Huan Zhang,
Qinghua Shi
Publication year - 2022
Publication title -
asian journal of andrology/asian journal of andrology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.701
H-Index - 74
eISSN - 1745-7262
pISSN - 1008-682X
DOI - 10.4103/aja202177
Subject(s) - sanger sequencing , cystic fibrosis , compound heterozygosity , vas deferens , cystic fibrosis transmembrane conductance regulator , infertility , disease gene identification , exome sequencing , male infertility , medicine , azoospermia , genetic testing , genetics , mutation , pathology , biology , gene , pregnancy