Presku: | AAP41739 |
Size: | 100 ug |
Weight: | 86kDa |
Gene: | 5172 |
Format: | Lyophilized powder |
Target: | 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 S |
Alternative names: | DFNB4; PDS |