Pds antibody, DFNB4 antibody, EVA antibody, PDS antibody, TDH2B antibody, pendrin antibody, solute carrier family 26 member 4 antibody, solute carrier family 26, member 4 antibody, SLC26A4 antibody, Slc26a4 antibody
背景
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.,SLC26A4;DFNB4;EVA;PDS;TDH2B;pendrin,Cancer,Signal Transduction,Endocrine & Metabolism,Neuroscience,SLC26A4