Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Deafness, non-syndromic, autosomal recessive

Hum Genet. 2010 Jan;127(1):116.
No abstract available

MeSH terms

  • Codon / genetics
  • Consanguinity
  • Deafness / genetics*
  • Family Health
  • Female
  • Genes, Recessive
  • Humans
  • Iron
  • Male
  • Membrane Transport Proteins / genetics*
  • Mutation, Missense*
  • Sulfate Transporters

Substances

  • Codon
  • Membrane Transport Proteins
  • SLC26A4 protein, human
  • Sulfate Transporters
  • Iron