PMC:516044 / 0-320 JSONTXT

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{"target":"https://pubannotation.org/docs/sourcedb/PMC/sourceid/516044","sourcedb":"PMC","sourceid":"516044","source_url":"http://www.ncbi.nlm.nih.gov/pmc/516044","text":"Loss of KCNJ10 protein expression abolishes endocochlear potential and causes deafness in Pendred syndrome mouse model\n\nAbstract\nBackground\nPendred syndrome, a common autosomal-recessive disorder characterized by congenital deafness and goiter, is caused by mutations of SLC26A4, which codes for pendrin. 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