Molecular basis of red cell membrane disorders

Acta Haematologica

Volumn 108, Issue 4, 2002, Pages 210-218

  Delaunay, Jean ^a  

^a BICÊTRE HOSPITAL   (France)

Author keywords

Hereditary elliptocytosis and poikilocytosis; Hereditary spherocytosis; Hereditary stomatocytoses; Southeast Asian ovalocytosis

Indexed keywords

ANKYRIN; ERYTHROCYTE BAND 3 PROTEIN; ERYTHROCYTE BAND 4.1 PROTEIN; ERYTHROCYTE BAND 4.2 PROTEIN; FODRIN; MONOVALENT CATION; PROTEIN SUBUNIT; SPECTRIN BETA; TETRAMER; UNCLASSIFIED DRUG;

ARTICLE; CELL MEMBRANE PERMEABILITY; DEHYDRATED HEREDITARY STOMATOCYTOSIS; EDEMA; ERYTHROCYTE DISORDER; ERYTHROCYTE FRAGILITY; FAMILIAL PSEUDOHYPERKALEMIA; GENE DELETION; GENE LOCATION; GENE MAPPING; GENE MUTATION; GENETIC CODE; GENETIC POLYMORPHISM; HEREDITARY ELLIPTOCYTOSIS; HEREDITARY SPHEROCYTOSIS; HUMAN; HYPERKALEMIA; KIDNEY TUBULE ACIDOSIS; MOLECULAR CLONING; NUCLEOTIDE SEQUENCE; OVERHYDRATED HEREDITARY STOMATOCYTOSIS; POIKILOCYTOSIS; PRIORITY JOURNAL; PROTEIN SYNTHESIS; SOUTHEAST ASIAN OVALOCYTOSIS; SPLENECTOMY; THROMBOEMBOLISM;

ANEMIA, HEMOLYTIC, CONGENITAL; ERYTHROCYTE MEMBRANE; ERYTHROCYTES, ABNORMAL; HUMANS; MEMBRANE PROTEINS; MUTATION;

EID: 0036432768     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000065657     Document Type: Article

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