Functional Characterization of Wild-Type and a Mutated Form of SLC26A4 Identified in a Patient with Pendred Syndrome

Publisher: Karger

E-ISSN: 1421-9778|17|5-6|245-256

ISSN: 1015-8987

Source: Cellular Physiology and Biochemistry, Vol.17, Iss.5-6, 2006-06, pp. : 245-256

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Abstract