A rare frameshift variant in trans with the IVS9-5T allele of CFTR in a Chinese pedigree with congenital aplasia of vas deferens. [electronic resource]
- Journal of assisted reproduction and genetics Dec 2019
- 2541-2545 p. digital
Publication Type: Journal Article
1573-7330
10.1007/s10815-019-01617-4 doi
Adult Alleles Azoospermia--epidemiology China--epidemiology Cystic Fibrosis Transmembrane Conductance Regulator--genetics Female Frameshift Mutation--genetics Genetic Testing Humans Infertility, Male--epidemiology Male Male Urogenital Diseases--epidemiology Pedigree Vas Deferens--abnormalities