S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded protein
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S26A4 Polyclonal Antibody, 50ul Sample Library Tubes Studies determined the encoded proteinMutations 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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