Please use this identifier to cite or link to this item: http://hdl.handle.net/10316/45542
Title: 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)?)
Authors: Bento, Celeste 
Almeida, Helena 
Maia, Tabita M. 
Relvas, Luís 
Oliveira, Ana C. 
Rossi, Cédric 
Girodon, François 
Fernandez-Lago, Carlos 
Aguado-Diaz, Ascension 
Fraga, Cristina 
Costa, Ricardo M. 
Araújo, Ana L. 
Silva, João 
Vitória, Helena 
Miguel, Natalina 
Silveira, Maria Pedro 
Martin-Nuñez, Guillermo 
Ribeiro, Maria Letícia 
Issue Date: 2013
Serial title, monograph or event: European Journal of Haematology
URI: http://hdl.handle.net/10316/45542
ISSN: 09024441
DOI: 10.1111/ejh.12170
Rights: openAccess
Appears in Collections:I&D CIAS - Artigos em Revistas Internacionais

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