Complex interaction of hemoglobin (Hb) Nakhon Ratchasima [α63(E12)Ala→Val], a novel α2-globin chain variant with Hb E [β26(B8)Glu→Lys] and a deletional α+-thalassemia

Author:

Srivorakun Hataichanok,Fucharoen Goonnapa,Puangplruk Rawiwan,Kheawon Napat,Fucharoen Supan

Publisher

Wiley

Subject

Hematology,General Medicine

Reference18 articles.

1. Hemoglobinopathies in Southeast Asia;Fucharoen;Hemoglobin,1987

2. Detection and structural analysis of abnormal hemoglobins found in Thailand;Svasti;Southeast Asian J Trop Med Public Health,1999

3. Hb Paksé [(α2) codon 142 (TAA-TAT or Term-Tyr)] in Thai patients with EABart’s disease and Hb H disease;Sanchaisuriya;Hemoglobin,2002

4. Unstable and thalassemic alpha chain hemoglobin variants: a cause of Hb H disease and thalassemia intermedia;Wajcman;Hemoglobin,2008

5. A simplified screening strategy for thalassemia and haemoglobin E in rural communities of Southeast Asia;Fucharoen;Bull World Health Organ,2004

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