Spectrin mutations in hereditary elliptocytosis and hereditary spherocytosis

Human Mutation

Volumn 8, Issue 2, 1996, Pages 97-107

  Maillet, Philippe ^a   Alloisio, Nicole ^a   Morlé, Laurette ^a   Delaunay, Jean ^a  

^a CNRS   (France)

Author keywords

Hereditary elliptocytosis; Hereditary spherocytosis; Spectrin mutations

Indexed keywords

COMPLEMENTARY DNA; FODRIN; SPECTRIN;

ALLELE; ARTICLE; ERYTHROCYTE DEFORMABILITY; ERYTHROCYTE MEMBRANE; ETHNIC GROUP; GENE MUTATION; HEMOLYSIS; HEREDITARY ELLIPTOCYTOSIS; HEREDITARY SPHEROCYTOSIS; HUMAN; HUMAN CELL; PHENOTYPE; POLYACRYLAMIDE GEL ELECTROPHORESIS; PRIORITY JOURNAL; SINGLE STRAND CONFORMATION POLYMORPHISM;

ELLIPTOCYTOSIS, HEREDITARY; ERYTHROCYTE MEMBRANE; HUMANS; MUTATION; POLYMORPHISM, SINGLE-STRANDED CONFORMATIONAL; SPHEROCYTOSIS, HEREDITARY;

EID: 0029764793     PISSN: 10597794     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1098-1004(1996)8:2<97::AID-HUMU1>3.0.CO;2-M     Document Type: Article

References (10)

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