A novel splicing variant in the TMC1 gene causes non-syndromic hearing loss in a Chinese family

Chin Med J (Engl). 2022 Nov 5;135(21):2631-2633. doi: 10.1097/CM9.0000000000001966.
No abstract available

Publication types

  • Letter

MeSH terms

  • Asian People / genetics
  • Deafness*
  • East Asian People
  • Hearing Loss, Sensorineural* / genetics
  • Humans
  • Membrane Proteins / genetics
  • Mutation
  • Pedigree

Substances

  • TMC1 protein, human
  • Membrane Proteins

Supplementary concepts

  • Nonsyndromic Deafness