Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene.

Annals of hematology - 1 Sept 2008

Ru Yong Xi, Zhu Xiao-fan, Yan Wen-wei, Gao Jing-tao, Schwarz Klaus, Heimpel Hermann

Abstract excerpt

Congenital dyserythropoietic anemia I (CDA I) is a well-defined entity within the heterogeneous group of the CDAs. So far, most CDA cases were reported from Europe and Israel. A homozygous mutation of the CDAN1-gene was identified from a founder population observed in Bedouin tribes in Israel, an...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anemia, Dyserythropoietic, Congenital
Share to Bone Marrow Cells
Share to China

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Erythroblasts

Share to Glycoproteins

Share to Mutation

Share to Nuclear Family

Share to Nuclear Proteins

Source

Identifiers

PMID: 18575862
DOI: 10.1007/s00277-008-0519-3

Genes

CDA
CDAN1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-18575862-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Congenital dyserythropoietic anemia in a Chinese family with a mutation of the CDAN1-gene.PMID 18575862Read ↗

Congenital dyserythropoietic anemia in China: a case report from two families and a review.Semantic proximity Read ↗

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1.Semantic proximity Read ↗

Congenital dyserythropoiesis anemia type Ia with a novel CDAN1 mutation diagnosed by whole exome sequencing.Semantic proximity Read ↗

Congenital dyserythropoietic anemia type I mimicking myelodysplasia syndrome with a novel CDAN1 mutation.Semantic proximity Read ↗

Congenital dyserythropoietic anemia type 1 with a novel mutation in the CDAN1 gene previously diagnosed as congenital hemolytic anemia.Semantic proximity Read ↗

Molecular and cellular characterization of congenital dyserythropoietic anaemia type 1Semantic proximity Read ↗

Congenital dyserythropoietic anemia type I with bone abnormalities, mutations of the CDAN I gene, and significant responsiveness to alpha-interferon therapy.Semantic proximity Read ↗

Clinical and molecular variability in congenital dyserythropoietic anaemia type I.Semantic proximity Read ↗

A case of congenital dyserythropoietic anemia type 1 in a Japanese adult with a CDAN1 gene mutation and an inappropriately low serum hepcidin-25 level.Semantic proximity Read ↗

Congenital dyserythropoietic anemia type I (CDA I): molecular genetics, clinical appearance, and prognosis based on long-term observation.Semantic proximity Read ↗

The complete complement of C1q-domain-containing proteins in Homo sapiens.Semantic proximity Read ↗

Mutations in the homeodomain of HOXD13 cause syndactyly type 1-c in two Chinese families.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.