Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation --SEA/--CR, a novel α0-thalassemia deletion

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Bibliographic Details
Main Authors:	Chedtapak Ruengdit, Sitthichai Panyasai, Naowarat Kunyanone, Worawich Phornsiricharoenphant, Chumpol Ngamphiw, Sissades Tongsima, Orapan Sripichai, Serge Pissard, Sakorn Pornprasert
Format:	Journal
Published:	2020
Subjects:	Biochemistry, Genetics and Molecular Biology Medicine
Online Access:	https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85077975755&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/68275
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Institution:	Chiang Mai University

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Characterization and identification of Hb Bart’s hydrops fetalis caused by a compound heterozygous mutation --<sup>SEA</sup>/--<sup>CR</sup>, a novel α<sup>0</sup>-thalassemia deletion