Zamzureena Mohd Rani

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

R. Jamal, L. Wu, N. A. Abdul Murad, 2017, Orphanet Journal of Rare Diseases.

Hypercholesterolemia in the Malaysian Cohort Participants: Genetic and Non-Genetic Risk Factors

R. Jamal, S. A. Sulaiman, N. A. Abdul Murad, 2023, Genes.