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Abnova
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Sequence of this protein is as follows: RSLRVIVKEF QRIDVNVYFA SLQDYVIEKL EQCGFFDDNI RKDTFFLTVH DAILYLQNQV KSQEGQGSIL ETITLIQDCK D
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.
仅用于科研。不用于诊断过程。未经明确授权不得转售。