May band 3 hyper-phosphorylation have a functional role in microcyte formation in heterozygous thalassemias?

Blood Cells, Molecules, and Diseases

Volumn 45, Issue 1, 2010, Pages 65-66

  Ferru, Emanuela ^a   Pantaleo, Antonella ^b   Mannu, Franca ^c   Carta, Franco ^c   Turrini, Franco ^b  

^a UNIVERSITY OF VERONA   (Italy)

^b UNIVERSITY OF TURIN   (Italy)

^c Nurex   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA GLOBIN; ERYTHROCYTE BAND 3 PROTEIN; GLOBIN;

BETA THALASSEMIA; BINDING AFFINITY; HETEROZYGOTE; HUMAN; LETTER; MEAN CORPUSCULAR VOLUME; MICROCYTOSIS; PRIORITY JOURNAL; PROTEIN AGGREGATION; PROTEIN BINDING; PROTEIN PHOSPHORYLATION; PROTEIN VARIANT; THALASSEMIA;

ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; ERYTHROCYTES, ABNORMAL; HETEROZYGOTE; HUMANS; PHOSPHORYLATION; THALASSEMIA;

EID: 77953133958     PISSN: 10799796     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bcmd.2010.02.018     Document Type: Letter

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