Enhanced haemolysis with β-thalassaemia trait due to the unstable β chain variant, Hb Gunma, accompanied by hereditary elliptocytosis due to protein 4·1 deficiency in a Japanese family-Reference-Cited by-同舟云学术

Enhanced haemolysis with β-thalassaemia trait due to the unstable β chain variant, Hb Gunma, accompanied by hereditary elliptocytosis due to protein 4·1 deficiency in a Japanese family

Published:2002-03-25 Issue:1 Volume:117 Page:193-197
ISSN:0007-1048
Container-title:British Journal of Haematology
language:en
Short-container-title:

Author:

Maehara Tadashi,Tsukamoto Norifumi,Nojima Yoshihisa,Karasawa Masamitsu,Murakami Hirokazu,Hattori Yukio,Ideguchi Hiroshi

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2141.2002.03338.x/fullpdf

Reference25 articles.

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2. The combination of hereditary elliptocytosis with heterozygous beta-thalassaemia;Aksoy;Acta Haematologica (Basel),1963

3. Combination of hereditary elliptocytosis and heterozygous β-thalassaemia: a family study;Aksoy;Journal of Medical Genetics,1968

4. Abnormal assembly of membrane proteins in erythroid progenitors of patients with β-thalassemia major;Aljurf;Blood,1996

5. Hereditary elliptocytosis associated with heterozygous beta-thalassemia. A study in a Greek family;Angelopoulos;Annales Paediatrici (Basel),1965

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