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)?). (Q45897769)
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scientific article published on 20 August 2013
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | 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)?). |
scientific article published on 20 August 2013 |
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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)?). (English)
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Helena Almeida
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Tabita M Maia
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Luís Relvas
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Ana C Oliveira
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Cédric Rossi
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François Girodon
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Carlos Fernandez-Lago
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Ascension Aguado-Diaz
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Ricardo M Costa
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Ana L Araújo
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João Silva
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Helena Vitória
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Natalina Miguel
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Maria Pedro Silveira
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Guillermo Martin-Nuñez
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20 August 2013
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91
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4
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361-368
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