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Shao-Min Wu, Chan Li, Su-Ran Huang, Fan Jiang & Dong-Zhi Li. (2024) A 6-Year Follow-up of a Chinese Child with Homozygous β0-Thalaasemia and a Heterozygous KLF1 Mutation. Hemoglobin 48:1, pages 60-62.
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Chattree Hantaweepant, Bhoom Suktitipat, Manop Pithukpakorn, Yingyong Chinthammitr, Chanin Limwongse, Nawaporn Tansiri, Surasak Sawatnatee, Chayamon Takpradit, Wannaphorn Rotchanapanya, Saranya Pongudom, Kanyaporn Charoenprasert, Kittiphong Paiboonsukwong, Wichuda Thamprasert, Narumol Nolwachai, Wanlapa Rattanasawat, Busakorn Sae-Aeng, Nisachon Khorwanichakij, Putchong Saetow, Supawee Saengboon, Krittichat Kamjornpreecha, Wikanda Pholmoo, Boonyanuch Dujjawan & Noppadol Siritanaratkul. (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.
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Articles from other publishers (2)
M. N. Gnanapragasam, A. Planutis, J. A. Glassberg & J. J. Bieker. (2023) Identification of a genomic DNA sequence that quantitatively modulates KLF1 transcription factor expression in differentiating human hematopoietic cells. Scientific Reports 13:1.
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Tanu Tangsricharoen, Rungrote Natesirinilkul, Arunee Phusua, Kanda Fanhchaksai, Chupong Ittiwut, Wanna Chetruengchai, Monthana Juntharaniyom, Pimlak Charoenkwan, Vip Viprakasit, Chureerat Phokaew & Vorasuk Shotelersuk. (2021)
Severe neonatal haemolytic anaemia caused by compound heterozygous
KLF1
mutations: report of four families and literature review
. British Journal of Haematology 194:3, pages 626-634.
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