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Title: 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
Authors: Chupong Ittiwut
Rungrote Natesirinilkul
Fuanglada Tongprasert
Lalita Sathitsamitphong
Chane Choed-amphai
Kanda Fanhchaksai
Pimlak Charoenkwan
Kanya Suphapeetiporn
Vorasuk Shotelersuk
Keywords: Medicine
Issue Date: 1-Jan-2018
ISSN: 13652141
Appears in Collections:CMUL: Journal Articles

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