Oral Session 2-9D Hemolytic anemia

[OS2-9D-2] Coinherited biallelic mutation of SPTB and β-thalassemia trait causes severe hemolytic anemia

Pimlak Charoenkwan¹, Chupong Ittiwut^2,3, Rungrote Natesirinilkul¹, Lalita Sathitsamitpong¹, Arunee Phusua¹, Kanda Fanhchaksai¹, Supan Fucharoen⁴, Kanya Suphapeetiporn^2,3, Vorasuk Shotelersuk^2,3 (1.Department of Pediatrics, Faculty of Medicine, Chiang Mai University, Muang, Kingdom of Thailand, 2.Department of Pediatrics, Faculty of Medicine, Center of Excellence for Medical Genomics, Chulalongkorn University, Pathumwan, Kingdom of Thailand, 3.Excellence Center for Medical Genetics, King Chulalongkorn Memorial Hospital, The Thai Red Cross Society, Pathumwan, Kingdom of Thailand, 4.Centre for Research and Development of Medical Diagnostic Laboratories (CMDL), Faculty of Associated Medical Sciences, Khon Kaen University, Muang, Kingdom of Thailand)