Novel mutations in SPTA1 and SPTB identified by whole exome sequencing in eight Thai families with hereditary pyropoikilocytosis presenting with severe fetal and neonatal anaemia

British Journal of Haematology, EarlyView.

Source: British Journal of Haematology - September 10, 2018 Category: Hematology Authors: Chupong Ittiwut , Rungrote Natesirinilkul , Fuanglada Tongprasert , Lalita Sathitsamitphong , Chane Choed ‐amphai , Kanda Fanhchaksai , Pimlak Charoenkwan , Kanya Suphapeetiporn , Vorasuk Shotelersuk Source Type: research