SCNN1B and CA12 play vital roles in occurrence of congenital bilateral absence of vas deferens (CBAVD)

Asian J Androl. 2019 Sep-Oct;21(5):525-527. doi: 10.4103/aja.aja_112_18.
No abstract available

Publication types

  • Letter

MeSH terms

  • Adult
  • Azoospermia / genetics
  • Azoospermia / pathology
  • Carbonic Anhydrases / genetics*
  • Congenital Abnormalities / epidemiology
  • 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*

Substances

  • Epithelial Sodium Channels
  • SCNN1B protein, human
  • Carbonic Anhydrases
  • carbonic anhydrase XII

Supplementary concepts

  • Congenital bilateral aplasia of vas deferens