Novel human pathological mutations. Gene symbol: SLC26A4. Disease: Pendred syndrome

Hum Genet. 2010 Apr;127(4):468-9.
No abstract available

MeSH terms

  • Base Sequence
  • Codon / genetics
  • Consanguinity
  • Frameshift Mutation
  • Goiter, Nodular / genetics
  • Hearing Loss, Sensorineural / genetics
  • Humans
  • Iran
  • Membrane Transport Proteins / genetics*
  • Sequence Deletion
  • Sulfate Transporters

Substances

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

Supplementary concepts

  • Pendred syndrome