Homozygous missense mutation (band 3 Fukuoka: G130R): a mild form of hereditary spherocytosis with near‐normal band 3 content and minimal changes of membrane ultrastructure despite moderate protein 4.2 deficiency

Author:

Inoue Takafumi1,Kanzaki Akio1,Kaku Mayumi1,Yawata Ayumi1,Takezono Masami1,Okamoto Naoto1,Wada Hideho1,Sugihara Takashi1,Yamada Osamu1,Katayama Yasuyuki2,Nagata Naokazu2,Yawata Yoshihito1

Affiliation:

1. Division of Haematology, Department of Medicine, Kawasaki Medical School, Kurashiki City, Japan,

2. The Third Department of Medicine, National Defence Medical College, Tokorozawa, Japan

Publisher

Wiley

Subject

Hematology

Reference22 articles.

1. Analysis of the oligomeric state of band 3, the anion transport protein of the human erythrocyte membrane, by size exclusion high performance chromatography: oligomeric stability and origin of heterogeneity;Casey J.R.;Journal of Biological Chemistry,1991

2. Electrophoretic analysis of the major polypeptides of the human erythrocyte membrane

3. Gallagher P.G. Forget B.G. Lux S.E.(1998) Disorders of the erythrocyte membrane.Hematology of Infancy and Childhood(ed. by D. G. Nathan and S. H. Orkin) pp.544664. Saunders Philadelphia.

4. Control of band 3 lateral and rotational mobility by band 4.2 in intact erythrocytes: release of band 3 oligomers from low-affinity binding sites

5. Abnormal band 3 protein (band 3 Fukuoka) found in two cases of erythrocyte band 4.2 deficiency. (Abstract);Ideguchi H.;International Journal of Hematology,1994

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