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

Hum Genet. 2010 Apr;127(4):471.
No abstract available

MeSH terms

  • Amino Acid Substitution
  • Base Sequence
  • Codon / genetics
  • Consanguinity
  • Deafness / genetics*
  • Humans
  • Iran
  • Membrane Transport Proteins / genetics*
  • Mutation, Missense
  • Sulfate Transporters

Substances

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