Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family

por Chow, Yock-Ping, Abdul Murad, Nor Azian, Mohd Rani, Zamzureena, Khoo, Jia-Shiun, Chong, Pei-Sin, Wu, Loo-Ling, Jamal, Rahman
Publicado 2017