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)?)

Please use this identifier to cite or link to this item: https://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:	https://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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