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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