Congenital dyserythropoietic anemia type I (CDAI): Molecular genetics, clinical appearance, and prognosis based on long-term observation

Blood

Volumn 107, Issue 1, 2006, Pages 334-340

  Heimpel, Hermann ^a   Schwarz, Klaus ^b   Ebnöther, Monika ^b   Goede, Jeroen S ^b   Heydrich, Detlev ^b   Kamp, Torsten ^b   Plaumann, Lothar ^b   Rath, Bettina ^b   Roessler, Jochen ^b   Schildknecht, Otto ^b   Schmid, Mathias ^b   Wuillemin, Walter ^b   Einsiedler, Beate ^b   Leichtle, Rosi ^b   Tamary, Hannah ^b   Kohne, Elisabeth ^b  

^a UNIVERSITY OF ULM   (Germany)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA2A INTERFERON; CODANIN 1 PROTEIN; HEMOGLOBIN; PROTEIN; UNCLASSIFIED DRUG;

ADOLESCENT; ADULT; AGE; AGE DISTRIBUTION; AMINO ACID SUBSTITUTION; ARTICLE; CHRONIC MACROCYTIC ANEMIA; CLINICAL ARTICLE; CLINICAL FEATURE; CLINICAL OBSERVATION; CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE 1; DISEASE SEVERITY; ERYTHROCYTE TRANSFUSION; EXON; FEMALE; FRAMESHIFT MUTATION; GALLSTONE; GENE DELETION; GENE MUTATION; HEMOGLOBIN DETERMINATION; HUMAN; IRON DEPLETION; MALE; MOLECULAR GENETICS; NUCLEOTIDE SEQUENCE; PRESCHOOL CHILD; PRIORITY JOURNAL; PROGNOSIS; SPLENECTOMY; TREATMENT OUTCOME;

EID: 30144440213     PISSN: 00064971     EISSN: 00064971     Source Type: Journal    
DOI: 10.1182/blood-2005-01-0421     Document Type: Article

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