Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)-Reference-Cited by-同舟云学术

Molecular study of congenital erythrocytosis in 70 unrelated patients revealed a potential causal mutation in less than half of the cases (Where is/are the missing gene(s)?)

Published:2013-08 Issue: Volume: Page:n/a-n/a
ISSN:0902-4441
Container-title:European Journal of Haematology
language:en
Short-container-title:Eur J Haematol

Author:

Bento Celeste¹,Almeida Helena¹,Maia Tabita M.¹,Relvas Luís¹,Oliveira Ana C.¹,Rossi Cédric²,Girodon François²,Fernandez-Lago Carlos³,Aguado-Diaz Ascension⁴,Fraga Cristina⁵,Costa Ricardo M.⁶,Araújo Ana L.⁵,Silva João⁵,Vitória Helena⁷,Miguel Natalina⁸,Silveira Maria Pedro⁹,Martin-Nuñez Guillermo¹⁰,Ribeiro Maria Letícia¹

Affiliation:

1. Serviço de Hematologia; Centro Hospitalar e Universitário de Coimbra; Coimbra; Portugal

2. Laboratoire d'Hématologie; Centre Hospitalier Universitaire Dijon; Dijon; France

3. Servicio de Hematoloxia; Complexo Hospitalario Universitário A Coruña; A Coruña; Spain

4. Servicio de Hematologia; Hospital Universitario Virgen del Rocio; Sevilla; Spain

5. Serviço de Hematologia; Hospital do Divino Espírito Santo; Ponta Delgada-Açores; Portugal

6. Unidade de Oncologia; Centro Hospitalar Barreiro Montijo; Barreiro; Portugal

7. Serviço de Hematologia; Centro Hospitalar Tondela-Viseu; Viseu; Portugal

8. Serviço de Pediatria; Centro Hospitalar Trás-os- Montes e Alto Douro; Vila Real; Portugal

9. Serviço de Hematologia; Centro Hospitalar Lisboa Oriental; Lisboa; Portugal

10. Servicio de Hematologia; Hospital Virgen del Puerto; Plasencia; Spain

Publisher

Wiley

Subject

Hematology,General Medicine

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/ejh.12170/fullpdf

Reference36 articles.

1. Pathophysiology of anemia and erythrocytosis;Hodges;Crit Rev Oncol Hematol,2007

2. Regulation of erythropoietin production;Jelkmann;J Physiol,2011

3. Benign erythrocytosis and other familial and congenital polycythemias;Prchal;Eur J Haematol,1996

4. The complete evaluation of erythrocytosis: congenital and acquired;Patnaik;Leukemia,2009

5. Genetic heterogeneity of primary familial and congenital polycythemia;Kralovics;Am J Hematol,2001

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