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Functional Characterization of Rare Genetic Variants in the N-Terminus of Complement Factor H in aHUS, C3G, and AMD.
Wong, Edwin K S; Hallam, Thomas M; Brocklebank, Vicky; Walsh, Patrick R; Smith-Jackson, Kate; Shuttleworth, Victoria G; Cox, Thomas E; Anderson, Holly E; Barlow, Paul Nigel; Marchbank, Kevin James; Harris, Claire L; Kavanagh, David.
Afiliação
  • Wong EKS; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Hallam TM; National Renal Complement Therapeutics Centre, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
  • Brocklebank V; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Walsh PR; National Renal Complement Therapeutics Centre, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
  • Smith-Jackson K; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Shuttleworth VG; National Renal Complement Therapeutics Centre, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
  • Cox TE; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Anderson HE; National Renal Complement Therapeutics Centre, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
  • Barlow PN; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Marchbank KJ; National Renal Complement Therapeutics Centre, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
  • Harris CL; Complement Therapeutics Research Group, Translational and Clinical Research Institute, Newcastle University, Newcastle upon Tyne, United Kingdom.
  • Kavanagh D; National Renal Complement Therapeutics Centre, Royal Victoria Infirmary, Newcastle upon Tyne, United Kingdom.
Front Immunol ; 11: 602284, 2020.
Article em En | MEDLINE | ID: mdl-33519811
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Glomerulonefrite Membranoproliferativa / Síndrome Hemolítico-Urêmica Atípica / Degeneração Macular Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Variação Genética / Glomerulonefrite Membranoproliferativa / Síndrome Hemolítico-Urêmica Atípica / Degeneração Macular Idioma: En Ano de publicação: 2020 Tipo de documento: Article