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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)?)  Full Text
AUTHORS: Celeste Bento; Helena Almeida; Tabita M Maia; Luis Relvas; Ana C Oliveira; Cedric Rossi; Francois Girodon; Carlos Fernandez Lago; Ascension Aguado Diaz; Cristina Fraga; Ricardo M Costa; Ana L Araujo; Joao Silva; Helena Vitoria; Natalina Miguel; Maria Pedro Silveira; Guillermo Martin Nunez; Maria Leticia Ribeiro ;
PUBLISHED: 2013, SOURCE: EUROPEAN JOURNAL OF HAEMATOLOGY, VOLUME: 91, ISSUE: 4
INDEXED IN: Scopus WOS CrossRef: 3