SLC26A4 gene mutation; solute carrier family 26 member 4 gene mutation; pendrin gene mutation

Clinical significance

• defects in SLC26A4 are a cause of:
  • Pendred syndrome
  • non-syndromic autosomal recessive neurosensory deafness 4

More general terms

• gene mutation testing; gene mutation analysis

Additional terms

• Pendrin; Na+-independent chloride/iodide transporter; solute carrier family 26 member 4 (SLC26A4, PDS)