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Effect of rare coding variants in the CFI gene on Factor I expression levels.
de Jong, Sarah; Volokhina, Elena B; de Breuk, Anita; Nilsson, Sara C; de Jong, Eiko K; van der Kar, Nicole C A J; Bakker, Bjorn; Hoyng, Carel B; van den Heuvel, Lambert P; Blom, Anna M; den Hollander, Anneke I.
Afiliação
  • de Jong S; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • Volokhina EB; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • de Breuk A; Amalia Children's Hospital, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • Nilsson SC; Department of Laboratory Medicine, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • de Jong EK; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • van der Kar NCAJ; Department of Translational Medicine, Lund University, 21428 Malmö, Sweden.
  • Bakker B; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • Hoyng CB; Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • van den Heuvel LP; Amalia Children's Hospital, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • Blom AM; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
  • den Hollander AI; Department of Ophthalmology, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Hum Mol Genet ; 29(14): 2313-2324, 2020 08 11.
Article em En | MEDLINE | ID: mdl-32510551
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrinogênio / Fator I do Complemento / Síndrome Hemolítico-Urêmica Atípica / Degeneração Macular Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Fibrinogênio / Fator I do Complemento / Síndrome Hemolítico-Urêmica Atípica / Degeneração Macular Tipo de estudo: Prognostic_studies Limite: Aged / Aged80 / Female / Humans / Male / Middle aged Idioma: En Revista: Hum Mol Genet Assunto da revista: BIOLOGIA MOLECULAR / GENETICA MEDICA Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Holanda