Heterozygosity of CDAN II (HEMPAS) gene may be detected by the analysis of erythrocyte membrane glycoconjugates from healthy carriers

Haematologica

Volumn 87, Issue 2, 2002, Pages 126-130

  Zdebska, Ewa ^a   Mendek Czajkowska, Ewa ^a   Ploski, Rafal ^a   Woêniewicz, Bohdan ^a   Koscielak, Jerzy ^a  

^a INSTITUTE OF HEMATOLOGY AND TRANSFUSION MEDICINE   (Poland)

Author keywords

CDA II; Glycoconjugate abnormalities; Heterozygosity

Indexed keywords

ARTICLE; ERYTHROCYTE MEMBRANE; GENETIC LINKAGE; GENETIC SCREENING; HEREDITARY HEMOLYTIC ANEMIA; HETEROZYGOTE DETECTION; HUMAN; PATHOGENESIS; PEDIGREE;

ADULT; ANEMIA, DYSERYTHROPOIETIC, CONGENITAL; ANION EXCHANGE PROTEIN 1, ERYTHROCYTE; BIOLOGICAL MARKERS; BLOOD PROTEIN ELECTROPHORESIS; CERAMIDES; CHILD; ERYTHROCYTE MEMBRANE; FEMALE; GLYCOCONJUGATES; GLYCOPHORIN; GLYCOSYLATION; HETEROZYGOTE DETECTION; HUMANS; MALE; PEDIGREE; PROTEIN PROCESSING, POST-TRANSLATIONAL;

EID: 0036174697     PISSN: 03906078     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (20)

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5. Localization of the congenital dyserythropoietic anemia II locus to chromosome 20q11.2 by genomewide search
6. Localization of the gene for congenital dyserythropoietic anemia type III, CDAN3, to chromosome 15q21-q25
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9. Glycophorin A in two patients with congenital dyserythropoietic anemia type I and type II is partly unglycosylated
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