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NCBI Description of SLC26A4 |
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. |
Community Annotation of SLC26A4 Add / Edit SLC26A4: Annotations
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Figure notes
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Data details