Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study

Detalhes bibliográficos
Autor(a) principal: Manco, Licínio
Data de Publicação: 2016
Outros Autores: Bento, Celeste, Victor, Bruno L., Pereira, Janet, Relvas, Luís, Brito, Rui M., Seabra, Carlos, Maia, Tabita M., Ribeiro, M. Letícia
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/45864
https://doi.org/10.1016/j.bcmd.2016.06.002
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spelling Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study2016info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/45864http://hdl.handle.net/10316/45864https://doi.org/10.1016/j.bcmd.2016.06.002eng10799796Manco, LicínioBento, CelesteVictor, Bruno L.Pereira, JanetRelvas, LuísBrito, Rui M.Seabra, CarlosMaia, Tabita M.Ribeiro, M. Letíciainfo:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2020-05-29T09:42:17Zoai:estudogeral.uc.pt:10316/45864Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:52:37.783205Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
title Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
spellingShingle 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
title_short Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
title_full Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
title_fullStr Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
title_full_unstemmed Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
title_sort Hereditary nonspherocytic hemolytic anemia caused by red cell glucose-6-phosphate isomerase (GPI) deficiency in two Portuguese patients: Clinical features and molecular study
author Manco, Licínio
author_facet Manco, Licínio
Bento, Celeste
Victor, Bruno L.
Pereira, Janet
Relvas, Luís
Brito, Rui M.
Seabra, Carlos
Maia, Tabita M.
Ribeiro, M. Letícia
author_role author
author2 Bento, Celeste
Victor, Bruno L.
Pereira, Janet
Relvas, Luís
Brito, Rui M.
Seabra, Carlos
Maia, Tabita M.
Ribeiro, M. Letícia
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Manco, Licínio
Bento, Celeste
Victor, Bruno L.
Pereira, Janet
Relvas, Luís
Brito, Rui M.
Seabra, Carlos
Maia, Tabita M.
Ribeiro, M. Letícia
publishDate 2016
dc.date.none.fl_str_mv 2016
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/45864
http://hdl.handle.net/10316/45864
https://doi.org/10.1016/j.bcmd.2016.06.002
url http://hdl.handle.net/10316/45864
https://doi.org/10.1016/j.bcmd.2016.06.002
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10799796
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