Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects-Reference-Cited by-同舟云学术

Severe thalassemia syndrome caused by Hemoglobin Pak Num Po AEBart’s disease: A hematological, molecular, and diagnostic aspects

Published:2020-05-02 Issue:4 Volume:42 Page:
ISSN:1751-5521
Container-title:International Journal of Laboratory Hematology
language:en
Short-container-title:Int J Lab Hem

Author:

Singha Kritsada¹,Wiangnon Surapon²,Fucharoen Goonnapa¹,Jetsrisuparb Arunee³,Komwilaisak Patcharee³,Fucharoen Supan¹^ORCID

Affiliation:

1. Centre for Research and Development of Medical Diagnostic Laboratories Faculty of Associated Medical Sciences Khon Kaen University Khon Kaen Thailand

2. Faculty of Medicine Mahasarakham University Mahasarakham Thailand

3. Department of Pediatrics Faculty of Medicine Khon Kaen University Khon Kaen Thailand

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/ijlh.13224

Reference10 articles.

1. Genetic heterogeneity of hemoglobin AEBart's disease: A large cohort data from a single referral center in northeast Thailand

2. Co-inheritance of Hb Pak Num Po, a novel ?1 gene mutation, and ?0 thalassemia associated with transfusion-dependent Hb H disease

3. Variable Genotype-Phenotype Correlations in Patients With a Rare Nondeletional α-thalassemia; Hb Pak Num Po (HBA1

4. Prevention of severe thalassemia in northeast Thailand: 16 years of experience at a single university center

5. Clinical and hematologic manifestations of AEBart’s disease;Fucharoen S;Birth Defects Original Article Ser,1988

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