Search
SLC26A4 gene mutation; solute carrier family 26 member 4 gene mutation; pendrin gene mutation
Clinical significance:
- defects in SLC26A4 are a cause of:
a) Pendred syndrome
b) non-syndromic autosomal recessive neurosensory deafness 4
Related
Pendrin; Na+-independent chloride/iodide transporter; solute carrier family 26 member 4 (SLC26A4, PDS)
General
gene mutation testing; gene mutation analysis
References
Loinc