Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family
Crossref DOI link: https://doi.org/10.1186/s13023-017-0575-7
Published Online: 2017-02-21
Published Print: 2017-12
Update policy: https://doi.org/10.1007/springer_crossmark_policy
Chow, Yock-Ping
Abdul Murad, Nor Azian
Mohd Rani, Zamzureena
Khoo, Jia-Shiun
Chong, Pei-Sin
Wu, Loo-Ling
Jamal, Rahman
Funding for this research was provided by:
Universiti Kebangsaan Malaysia (PP-M-17KB001-0000000)
