SCNN1B and CA12 play vital roles in occurrence of congenital bilateral absence of vas deferens (CBAVD).
- Author:
Ying SHEN
1
;
Huan-Xun YUE
1
;
Fu-Ping LI
1
;
Feng-Yun HU
2
;
Xiao-Liang LI
1
;
Qian WAN
3
;
Wen-Rui ZHAO
1
;
Ji-Gang JING
4
;
Di-Ming CAI
4
;
Xiao-Hui JIANG
1
Author Information
- Publication Type:Letter
- MeSH: Adult; Azoospermia/pathology*; Carbonic Anhydrases/genetics*; Congenital Abnormalities/genetics*; Epithelial Sodium Channels/genetics*; Gene Expression Regulation/genetics*; Genome, Human; Humans; Infertility, Male/genetics*; Male; Male Urogenital Diseases/genetics*; Mutation; Vas Deferens/abnormalities*
- From: Asian Journal of Andrology 2019;21(5):525-527
- CountryChina
- Language:English
