Hantaweepant, C., Suktitipat, B., Pithukpakorn, M., Chinthammitr, Y., Limwongse, C., Tansiri, N., Sawatnatee, S., Takpradit, C., Rotchanapanya, W., Pongudom, S., Charoenprasert, K., Paiboonsukwong, K., Thamprasert, W., Nolwachai, N., Rattanasawat, W., Sae-Aeng, B., Khorwanichakij, N., Saetow, P., Saengboon, S., Kamjornpreecha, K., Pholmoo, W., Dujjawan, B., & Siritanaratkul, N. (2023). whole exome sequencing and rare variant association study to identify genetic modifiers, KLF1 mutations, and a novel double mutation in Thai patients with hemoglobin E/beta-thalassemia. Hematology, 28(1), . http://access.bl.uk/ark:/81055/vdc_100183604273.0x00001b