13023_2017_575_MOESM2_ESM.xlsx (94.32 kB)
Additional file 2: Table S1. of Exome sequencing identifies SLC26A4, GJB2, SCARB2 and DUOX2 mutations in 2 siblings with Pendred syndrome in a Malaysian family
dataset
posted on 2017-02-21, 05:00 authored by Yock-Ping Chow, Nor Azian Abdul Murad, Zamzureena Mohd Rani, Jia-Shiun Khoo, Pei-Sin Chong, Loo-Ling Wu, Rahman JamalList of non-synonymous heterozygous mutations inherited from father. (XLSX 94 kb)
