Clinical characteristics, laboratory features and genetic profile of hemoglobin E (HBB:c.79 G > A)/β (nucleotide -28 A > G) (HBB:c.-78 A > G) -thalassemia subjects identified from community- and hospital-recruited cohorts-Reference-Cited by-同舟云学术

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Clinical characteristics, laboratory features and genetic profile of hemoglobin E (HBB:c.79 G > A)/β (nucleotide -28 A > G) (HBB:c.-78 A > G) -thalassemia subjects identified from community- and hospital-recruited cohorts

Published:2024-11 Issue: Volume:109 Page:102883
ISSN:1079-9796
Container-title:Blood Cells, Molecules, and Diseases
language:en
Short-container-title:Blood Cells, Molecules, and Diseases

Author:

Chumnumsiriwath Piyatida,Charoenporn Prissana,Jermnim Sawichayaporn,Suannum Pawanrat,Samaisombat Monthira,Tapprom Akamon,Deoisares Rawisut,Wong Peerapon

Publisher

Elsevier BV

Reference20 articles.

1. Thalassemia in Thailand;Paiboonsukwong;Hemoglobin,2022

2. Lessons learned from a prenatal diagnosis program for thalassemia in Thailand;Wong;Prenat. Diagn.,2020

3. Beta-thalassemia in Thailand;Winichagoon;Ann. N. Y. Acad. Sci.,1990

4. Clinical manifestation of beta-thalassemia/hemoglobin E disease;Fucharoen;J. Pediatr. Hematol. Oncol.,2000

5. Molecular analysis of beta-globin gene mutations among Thai beta-thalassemia children: results from a single center study;Boonyawat;Appl. Clin. Genet.,2014

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