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[It has been shown that mutations of the SLC26A4 (PDS) gene were involved in syndromic deafness characterized by congenital sensorineural hearing impairment and goitre (Pendred's syndrome), as well as in congenital isolated deafness (DFNB4).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
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