Dominant and recessive SLC12A2-syndrome

Am J Med Genet A. 2022 Mar;188(3):996-999. doi: 10.1002/ajmg.a.62573. Epub 2021 Nov 19.
No abstract available

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Genes, Dominant
  • Genes, Recessive
  • Hearing Loss, Sensorineural* / genetics
  • Humans
  • Solute Carrier Family 12, Member 2 / genetics
  • Syndrome

Substances

  • SLC12A2 protein, human
  • Solute Carrier Family 12, Member 2