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Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study.
Manco, Licínio; Bento, Celeste; Victor, Bruno L; Pereira, Janet; Relvas, Luís; Brito, Rui M; Seabra, Carlos; Maia, Tabita M; Ribeiro, M Letícia.
  • Manco L; Department of Hematology, Centro Hospitalar e Universitário de Coimbra (CHUC), Coimbra, Portugal; Research Centre for Anthropology and Health (CIAS), Department of Life Sciences, University of Coimbra, Coimbra, Portugal. Electronic address: lmanco@antrop.uc.pt.
  • Bento C; Department of Hematology, Centro Hospitalar e Universitário de Coimbra (CHUC), Coimbra, Portugal; Research Centre for Anthropology and Health (CIAS), Department of Life Sciences, University of Coimbra, Coimbra, Portugal.
  • Victor BL; Chemistry Department, University of Coimbra, Coimbra, Portugal.
  • Pereira J; Research Centre for Anthropology and Health (CIAS), Department of Life Sciences, University of Coimbra, Coimbra, Portugal.
  • Relvas L; Research Centre for Anthropology and Health (CIAS), Department of Life Sciences, University of Coimbra, Coimbra, Portugal.
  • Brito RM; Chemistry Department, University of Coimbra, Coimbra, Portugal; Center for Neuroscience and Cell Biology, University of Coimbra, Coimbra, Portugal.
  • Seabra C; Serviço de Patologia Clínica, Hospital Infante D. Pedro, Aveiro, Portugal.
  • Maia TM; Department of Hematology, Centro Hospitalar e Universitário de Coimbra (CHUC), Coimbra, Portugal.
  • Ribeiro ML; Department of Hematology, Centro Hospitalar e Universitário de Coimbra (CHUC), Coimbra, Portugal; Research Centre for Anthropology and Health (CIAS), Department of Life Sciences, University of Coimbra, Coimbra, Portugal.
Blood Cells Mol Dis ; 60: 18-23, 2016 09.
Article en En | MEDLINE | ID: mdl-27519939
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Mutación Missense / Glucosa-6-Fosfato Isomerasa / Anemia Hemolítica Congénita no Esferocítica Tipo de estudio: Prognostic_studies Límite: Humans País como asunto: Europa Idioma: En Año: 2016 Tipo del documento: Article
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Mutación del Sistema de Lectura / Mutación Missense / Glucosa-6-Fosfato Isomerasa / Anemia Hemolítica Congénita no Esferocítica Tipo de estudio: Prognostic_studies Límite: Humans País como asunto: Europa Idioma: En Año: 2016 Tipo del documento: Article