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Issue Date
Title
Author(s)
1-Jan-2018
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
Chupong Ittiwut
;
Rungrote Natesirinilkul
;
Fuanglada Tongprasert
;
Lalita Sathitsamitphong
;
Chane Choed-amphai
;
Kanda Fanhchaksai
;
Pimlak Charoenkwan
;
Kanya Suphapeetiporn
;
Vorasuk Shotelersuk
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Author
1
Chane Choed-amphai
1
Chupong Ittiwut
1
Kanda Fanhchaksai
1
Kanya Suphapeetiporn
1
Lalita Sathitsamitphong
1
Rungrote Natesirinilkul
1
Vorasuk Shotelersuk