SLC26A4 mutation spectrum associated with DFNB4 deafness and Pendred's syndrome in Pakistanis.
Anwar S; Riazuddin S; Ahmed ZM; Tasneem S; Ateeq-ul-Jaleel; Khan SY; Griffith AJ; Friedman TB; Riazuddin S; Journal Of Human Genetics, 2009, vol. 54, issue 5, p 266, ISSN 1435232x. ISBN 1435232x.

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