Your browser doesn't support javascript.
loading
Pseudolinear C4d deposits in a hereditary glomerulopathy caused by a rare NC1 collagen-4-alpha-5 missense mutation: a "new disease entity"?
Roy, Sanjeet; Nalwa, Aasma; Keith, Jared; Weck, Karen; Singh, Harsharan; Nickeleit, Volker.
Afiliación
  • Roy S; Department of Pathology, Division of Nephropathology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
  • Nalwa A; Department of Pathology, Division of Nephropathology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
  • Keith J; Blue Ridge Nephrology and Hypertension Center, Boone, NC, USA.
  • Weck K; Department of Pathology, Molecular Genetics Laboratory, University of North Carolina at Chapel Hill, Chapel Hill, USA.
  • Singh H; Department of Pathology, Division of Nephropathology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
  • Nickeleit V; Department of Pathology, Division of Nephropathology, University of North Carolina at Chapel Hill, Chapel Hill, United States.
Ultrastruct Pathol ; 43(4-5): 209-215, 2019.
Article en En | MEDLINE | ID: mdl-31682783
Asunto(s)
Palabras clave
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Glomerulonefritis Membranosa / Complemento C4b / Colágeno Tipo IV Límite: Humans / Male / Middle aged Idioma: En Revista: Ultrastruct Pathol Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Fragmentos de Péptidos / Glomerulonefritis Membranosa / Complemento C4b / Colágeno Tipo IV Límite: Humans / Male / Middle aged Idioma: En Revista: Ultrastruct Pathol Año: 2019 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido