DOI:
10.1055/s-00046370
Global Medical Genetics
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References
Ben Said M, Dhouib H, BenZina Z. et al.
Segregation of a new mutation in SLC26A4 and p.E47X mutation in GJB2 within a consanguineous Tunisian family affected with Pendred syndrome.
Int J Pediatr Otorhinolaryngol 2012;
76 (06) 832-836
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