Jabba, Sairam V.; Oelke, Alisha; Singh, Ruchira; Maganti, Rajanikanth J.; Fleming, Sherry D.; Wall, Susan M.; Everett, Lorraine A.; Green, Eric D.; Wangemann, Antje Philine
(2013-10-15)
Background: Pendred syndrome, an autosomal-recessive disorder characterized by deafness and goiter, is caused by a mutation of SLC26A4, which codes for the anion exchanger pendrin. We investigated the relationship between ...