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)?)
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F. Girodon | C. Bento | C. Rossi | T. Maia | M. Ribeiro | H. Almeida | Ana C. Oliveira | C. Fernández-lago | Ascension Aguado-Diaz | Ana L. Araújo | João Silva | H. Vitória | Natalina Miguel | M. P. Silveira | G. Martín‐Nuñez | Ricardo Costa | Cristina Fraga | Luís Relvas