Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family-Reference-Cited by-同舟云学术

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Complex interaction of Hb Hekinan [α27(B8) Glu-Asp] and Hb E [β26(B8) Glu-Lys] with a deletional α-thalassemia 1 in a Thai family

Published:2003-04-15 Issue:5 Volume:70 Page:304-309
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:

Author:

Fucharoen Supan,Changtrakun Yossombat,Ratanasiri Thawalwong,Fucharoen Goonnapa,Sanchaisuriya Kanokwan

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1034/j.1600-0609.2003.00049.x/fullpdf

Reference29 articles.

1. Thalassemia in Thailand;Wasi;Ann NY Acad Sci,1980

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

3. An electrophoretically silent hemoglobin variant, Hb Hekinan [α27(B8)Glu-Asp] found in Japanese;Harano;Hemoglobin,1988

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1. A large cohort of Hb H disease in northeast Thailand: A molecular revisited, diverse genetic interactions and identification of a novel mutation;Clinica Chimica Acta;2024-07

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3. Compounded with hemoglobin Port Phillip and ‐α 4.2 or ‐‐ SEA deletions were identified in Chinese population;Molecular Genetics & Genomic Medicine;2021-08-16

4. α-Thalassemia Intermedia Results from Interactions of Unstable Hb Prato [α31(B12)Arg→Ser (HBA1 or HBA2 c.96G>T or C)] with the α-Thalassemia-1 [– –SEA (Southeast Asian)] Deletion in Thailand;Hemoglobin;2020-07-03

5. Novel interactions of two α-Hb variants with SEA deletion α0-thalassemia: hematological and molecular analyses;Hematology;2017-09-25

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