Hemoglobins F, A 2 , and E levels in Laotian children aged 6‐23 months with Hb E disorders: Effect of age, sex, and thalassemia types

Author:

Kingchaiyaphum Benchawan1,Sanchaisuriya Kanokwan2ORCID,Fucharoen Goonnapa2,Chaibunruang Attawut2,Hess Sonja Y.3,Hinnouho Guy‐Marino3,Barffour Maxwell A.3,Wessells Kimbery R.3,Kounnavong Sengchanh4,Fucharoen Supan2ORCID

Affiliation:

1. Graduate School Khon Kaen University Khon Kaen Thailand

2. Center for Research and Development of Medical Diagnostic Laboratories (CMDL) Faculty of Associated Medical Sciences Khon Kaen University Khon Kaen Thailand

3. Institute for Global Nutrition University of California Davis CA USA

4. Lao Tropical and Public Health Institute Ministry of Health Vientiane Lao

Funder

Bill and Melinda Gates Foundation

Publisher

Wiley

Subject

Biochemistry, medical,Clinical Biochemistry,Hematology,General Medicine

Reference28 articles.

1. Variation in fetal hemoglobin parameters and predicted hemoglobin S polymerization in sickle cell children in the first two years of life: Parisian Prospective Study on Sickle Cell Disease

2. Developmental changes in hemoglobin F levels during the first two years of life in normal and heterozygous beta‐thalassemia infants;Metaxotou‐Mavromati AD;Pediatrics,1982

3. Genetic modifiers of beta‐thalassemia;Thein SL;Haematologica,2005

4. The Switch from Fetal to Adult Hemoglobin

5. Abnormal RNA processing due to the exon mutation of βE-globin gene

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