S26A4 Polyclonal Antibody, 100ul Mammalian Expression with a role in targeting
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S26A4 Polyclonal Antibody, 100ul Mammalian Expression with a role in targetingMutations in this gene are associated with Pendred syndrome, the most common form of syndromic deafness, an autosomal recessive disease. It is highly homologous to the SLC26A3 gene; they have similar genomic structures and this gene is located 3' of the SLC26A3 gene. The encoded protein has homology to sulfate transporters.
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