目的囊性纤维化跨膜转导子基因(cystic fibrosis transmembrane conductance regulator,CFTR,OMIM602421)突变可以导致先天性双侧输精管缺如(congenital bilateral absence of the vas deferens,CBAVD,OMIM 277180)的发生,既往研究证明...
Dear Editor,Congenital bilateral absence of the vas deferens(CBAVD),a complete or partial defect of the Wolffian duct derivatives,is found in>25% of men with obstructive azoospermia(OA),but the underlying pathological...
先天性双侧输精管缺如(congenital bilateral absence of the vas deferens,CBAVD)目前认为主要由囊性纤维化跨膜转导子(cystic fibrosis transmembrane conductance regulator,CFTR)基因变异导致,在欧美国家CFTR基因变异检测已经用于...