Close to unraveling the secrets of congenital dyserythropoietic anemia types I and II

Haematologica

Volumn 94, Issue 5, 2009, Pages 599-602

  Iolascon, Achille ^a,b   Delaunay, Jean ^c  

^a UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^b CEINGE BIOTECNOLOGIE AVANZATE   (Italy)

^c BICÊTRE HOSPITAL   (France)

Author keywords

[No Author keywords available]

Indexed keywords

CODANIN 1; NUCLEAR PROTEIN; UNCLASSIFIED DRUG;

AUTOSOMAL RECESSIVE DISORDER; CDAN1 GENE; CLINICAL FEATURE; CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE 1; CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE 2; EDITORIAL; FETUS HYDROPS; GENE; GENE MUTATION; GLYCOSYLATION; HEMOLYTIC ANEMIA; HUMAN; JAUNDICE; SPLENOMEGALY; SYNDACTYLY;

ANEMIA, DYSERYTHROPOIETIC, CONGENITAL; E2F1 TRANSCRIPTION FACTOR; GATA1 TRANSCRIPTION FACTOR; GENETIC PREDISPOSITION TO DISEASE; GLYCOPROTEINS; HUMANS; MUTATION; PROTEIN BINDING;

EID: 66049131181     PISSN: 03906078     EISSN: 15928721     Source Type: Journal    
DOI: 10.3324/haematol.2009.005785     Document Type: Editorial

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