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

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
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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