AffiAB® S26A4 Rabbit Polyclonal Antibody
Cat#: AFG-EKA-11319
Size: 100 µL
Price:$246.00
Description
Mutations 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. [provided by RefSeq, Jul 2008],
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