DOI:
10.1055/s-00046370
Global Medical Genetics
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References
Chow YP, Abdul Murad NA, Mohd Rani Z. et al.
Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family.
Orphanet J Rare Dis 2017;
12 (01) 40
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