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)?)
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.,Langue:
english
Journal:
European Journal of Haematology
DOI:
10.1111/ejh.12170
Date:
August, 2013
Fichier:
PDF, 1.01 MB
english, 2013
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