Congenital dyserythropoietic anemia in China: a case report from two families and a review.

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Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: definition of clinical and molecular spectrum and identification of new diagnostic scores.

P2860

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Congenital dyserythropoietic anemia in China: a case report from two families and a review.

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2013 nî lūn-bûn

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2013年の論文

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年学术文章

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2013年學術文章

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2013年學術文章

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2013年學術文章

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name

Congenital dyserythropoietic a ...... rom two families and a review.

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type

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Congenital dyserythropoietic a ...... rom two families and a review.

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Congenital dyserythropoietic a ...... rom two families and a review.

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Congenital dyserythropoietic a ...... rom two families and a review.

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Brian Eyden

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Fengkui Zhang

http://www.w3.org/2001/XMLSchema#string

Gang Liu

http://www.w3.org/2001/XMLSchema#string

Guangjun Nie

http://www.w3.org/2001/XMLSchema#string

Huamei Zhang

http://www.w3.org/2001/XMLSchema#string

Jie Bai

http://www.w3.org/2001/XMLSchema#string

Neng Nie

http://www.w3.org/2001/XMLSchema#string

Shixuan Zhao

http://www.w3.org/2001/XMLSchema#string

Shuxu Dong

http://www.w3.org/2001/XMLSchema#string

Xiaofan Zhu

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P2860

Congenital dyserythropoietic anemia type I is caused by mutations in codanin-1

Molecular analysis of 42 patients with congenital dyserythropoietic anemia type II: new mutations in the SEC23B gene and a search for a genotype-phenotype relationship.

Clinical aspects and pathogenesis of congenital dyserythropoietic anemias: from morphology to molecular approach.

Mutational spectrum in congenital dyserythropoietic anemia type II: identification of 19 novel variants in SEC23B gene.

Congenital dyserythropoietic anemia type II - a case report of two siblings in a family

Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

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

Congenital dyserythropoietic anemia type III (CDA III) is caused by a mutation in kinesin family member, KIF23.

Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.

A Chinese family carrying novel mutations in SEC23B and HFE2, the genes responsible for congenital dyserythropoietic anaemia II (CDA II) and primary iron overload, respectively

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773-777

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scholarly article

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10.1007/S00277-013-1933-8

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2013-11-07T00:00:00Z

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258335453

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24196372

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P921

birth defect

Congenital dyserythropoietic anemia in China: a case report from two families and a review.

about

P2860

P2860

Congenital dyserythropoietic anemia in China: a case report from two families and a review.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921

P356

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P1476

P2093

P2860

P304

P31

P356

P433

P478

P577

P5875

P698

P921