Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/62841
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
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85053051054&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/62841
ISSN: 13652141
00071048
Appears in Collections:CMUL: Journal Articles

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