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Article

Congenital dyserythropoietic anemia type II: exclusion of seven candidate genes.

Blood cells, molecules & diseases - 1 Jan 2000

Lanzara Carmela, Ficarella Romina, Totaro Angela, Chen Xin, Roberto Roberta, Perrotta Silverio, Lasalandra Carla, Gasparini Paolo, Iolascon Achille, Carella Massimo

Abstract excerpt

Congenital dyserythropoietic anemias (CDA) are genetic disorders characterized by anemia and ineffective erythropoiesis. Three main types of CDA have been distinguished: CDA I, CDAII and CDA III, whose loci have been already mapped. After the identification of the locus for CDA II, also known as HEMPAS (hereditary erythroblast multinuclearity with positive acidified serum test), on the long arm of chromosome 20...

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Share to Anemia, Dyserythropoietic, Congenital
Share to Chromatography, High Pressure Liquid

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromosome Mapping

Share to Chromosomes, Human, Pair 20

Share to Erythrocytes

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Source

Identifiers

PMID: 12667984
DOI: 10.1016/s1079-9796(03)00009-3

Genes

CDA
ITCH
PLAGL2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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