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-thalass... by Hantaweepant, Chattree, Suktitipat, Bhoom, Pithukpakorn, Manop, Chinthammitr, Yingyong, Limwongse, Chanin, Tansiri, Nawaporn, Sawatnatee, Surasak, Takpradit, Chayamon, Rotchanapanya, Wannaphorn, Pongudom, Saranya, Charoenprasert, Kanyaporn, Paiboonsukwong, Kittiphong, Thamprasert, Wichuda, Nolwachai, Narumol, Rattanasawat, Wanlapa, Sae-Aeng, Busakorn, Khorwanichakij, Nisachon, Saetow, Putchong, Saengboon, Supawee, Kamjornpreecha, Krittichat, Pholmoo, Wikanda, Dujjawan, Boonyanuch, Siritanaratkul, Noppadol

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