Detection of gene mutations in patients with clinically suspected hereditary spherocytosis by NGS

Li Qin

Presentation information

Oral Session

Oral Session 1-9D Hemoglobinopathy

Fri. Oct 11, 2019 4:30 PM - 5:30 PM No.9 (Tokyo International Forum, 4F G402)

Chair: Hitoshi Kanno (Tokyo Women's Medical University Hospital, Transfusion Medicine and Cell Processing)

[OS1-9D-6] Detection of gene mutations in patients with clinically suspected hereditary spherocytosis by NGS

Li Qin^1,2, Yanbo Nie², Long Chen², Jing Li² (1.Institute of Hematology and Blood Disease Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, Tianjin, People's Republic of China, 2.Sino-US Diagnositics, Tianjin, People's Republic of China)

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