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ß6 integrinosis: a new lethal autosomal recessive ITGB6 disorder leading to impaired conformational transitions of the αVß6 integrin receptor.
Weil, Patrick; van den Bruck, Rhea; Ziegenhals, Thomas; Juranek, Stefan; Goedde, Daniel; Orth, Valerie; Wirth, Stefan; Jenke, Andreas C; Postberg, Jan.
Afiliación
  • Weil P; Clinical Molecular Genetics and Epigenetics, Centre for Biomedical Education and Research (ZBAF), HELIOS University Hospital Wuppertal, Witten/Herdecke University, Wuppertal, Germany.
  • van den Bruck R; Department of Paediatrics, HELIOS University Hospital Wuppertal, Wuppertal, Germany.
  • Ziegenhals T; Chair of Biochemistry, Theodor-Boveri-Institute at the Biocenter, University of Würzburg, Wurzburg, Germany.
  • Juranek S; Chair of Biochemistry, Theodor-Boveri-Institute at the Biocenter, University of Würzburg, Wurzburg, Germany.
  • Goedde D; Department of Pathology, HELIOS University Hospital Wuppertal, Wuppertal, Germany.
  • Orth V; Department of Surgery II, HELIOS University Hospital Wuppertal, Wuppertal, Germany.
  • Wirth S; Department of Paediatrics, HELIOS University Hospital Wuppertal, Wuppertal, Germany.
  • Jenke AC; Clinical Molecular Genetics and Epigenetics, Centre for Biomedical Education and Research (ZBAF), HELIOS University Hospital Wuppertal, Witten/Herdecke University, Wuppertal, Germany.
  • Postberg J; Department of Neonatology and General Pediatrics, Children's Hospital Kassel, Kassel, Germany.
Gut ; 69(7): 1359-1361, 2020 07.
Article en En | MEDLINE | ID: mdl-31201286

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Monocitos / Microbioma Gastrointestinal Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Monocitos / Microbioma Gastrointestinal Límite: Humans Idioma: En Año: 2020 Tipo del documento: Article