Plasma and red blood cell proteome in sickle-cell disease
Sickle-cell disease (SCD) is a clinically heterogeneous autosomal recessive monogenic chronic anaemia characterized by recurrent episodes of severe vaso-occlusion, haemolysis and infection. Painful crises are the major SCD clinical manifestation probably due to significant increase in dense red bloo...
| Autor principal: | |
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| Outros Autores: | , , , |
| Formato: | other |
| Idioma: | eng |
| Publicado em: |
2013
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| Assuntos: | |
| Texto completo: | http://hdl.handle.net/10400.18/1285 |
| País: | Portugal |
| Oai: | oai:repositorio.insa.pt:10400.18/1285 |