Retrospective cohort study of 205 cases with congenital dyserythropoietic anemia type II: Definition of clinical and molecular spectrum and identification of new diagnostic scores-Reference-Cited by-同舟云学术

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

Published:2014-07-22 Issue:10 Volume:89 Page:E169-E175
ISSN:0361-8609
Container-title:American Journal of Hematology
language:en
Short-container-title:Am. J. Hematol.

Author:

Russo Roberta¹²,Gambale Antonella¹²,Langella Concetta¹²,Andolfo Immacolata¹²,Unal Sule³,Iolascon Achille¹²

Affiliation:

1. Dipartimento di Medicina Molecolare e Biotecnologie Mediche; Università degli Studi di Napoli Federico II; Napoli Italy

2. CEINGE Biotecnologie Avanzate; Napoli Italy

3. Division of Pediatric Hematology; Hacettepe University; Ankara Turkey

Funder

Fondazione Telethon

Publisher

Wiley

Subject

Hematology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/ajh.23800/fullpdf

Reference23 articles.

1. Congenital dyserythropoietic anemias: Molecular insights and diagnostic approach;Iolascon;Blood,2013

2. The morphological diagnosis of congenital dyserythropoietic anemia: Results of a quantitative analysis of peripheral blood and bone marrow cells;Heimpel;Haematologica,2010

3. Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II;Schwarz;Nat Genet,2009

4. Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene;Bianchi;Hum Mutat,2009

5. Inherited hematological disorders due to defects in coat protein (COP)II complex;Russo;Am J Hematol,2013

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