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Loss of syntaxin 3 causes variant microvillus inclusion disease.
Wiegerinck, Caroline L; Janecke, Andreas R; Schneeberger, Kerstin; Vogel, Georg F; van Haaften-Visser, Désirée Y; Escher, Johanna C; Adam, Rüdiger; Thöni, Cornelia E; Pfaller, Kristian; Jordan, Alexander J; Weis, Cleo-Aron; Nijman, Isaac J; Monroe, Glen R; van Hasselt, Peter M; Cutz, Ernest; Klumperman, Judith; Clevers, Hans; Nieuwenhuis, Edward E S; Houwen, Roderick H J; van Haaften, Gijs; Hess, Michael W; Huber, Lukas A; Stapelbroek, Janneke M; Müller, Thomas; Middendorp, Sabine.
Affiliation
  • Wiegerinck CL; Division of Pediatrics, Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Janecke AR; Division of Human Genetics, Biocenter Innsbruck, Innsbruck, Austria; Department of Pediatrics I, Biocenter Innsbruck, Innsbruck, Austria.
  • Schneeberger K; Division of Pediatrics, Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Vogel GF; Division of Cell Biology, Biocenter Innsbruck, Innsbruck, Austria; Division of Histology and Embryology, Innsbruck Medical University, Innsbruck, Austria.
  • van Haaften-Visser DY; Division of Pediatrics, Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands; Department of Cell Biology, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Escher JC; Pediatric Gastroenterology, Sophia Children's Hospital, Erasmus MC, Rotterdam, The Netherlands.
  • Adam R; Pediatric Gastroenterology, Department of Pediatric and Adolescent Medicine, University Medical Centre, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Thöni CE; Division of Cell Biology, Biocenter Innsbruck, Innsbruck, Austria; Division of Pathology, Department of Pediatric Laboratory Medicine, Hospital for Sick Children, Toronto, Canada.
  • Pfaller K; Division of Histology and Embryology, Innsbruck Medical University, Innsbruck, Austria.
  • Jordan AJ; Pediatric Gastroenterology, Department of Pediatric and Adolescent Medicine, University Medical Centre, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Weis CA; Institute of Pathology, University Medical Centre, Medical Faculty Mannheim, Heidelberg University, Mannheim, Germany.
  • Nijman IJ; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Monroe GR; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van Hasselt PM; Division of Pediatrics, Department of Metabolic Diseases, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Cutz E; Division of Pathology, Department of Pediatric Laboratory Medicine, Hospital for Sick Children, Toronto, Canada.
  • Klumperman J; Department of Cell Biology, University Medical Center Utrecht, Utrecht, The Netherlands; University Medical Center Utrecht, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Clevers H; Hubrecht Institute for Developmental Biology and Stem Cell Research, Royal Dutch Academy of Sciences, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Nieuwenhuis EE; Division of Pediatrics, Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Houwen RH; Division of Pediatrics, Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • van Haaften G; Department of Medical Genetics, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Hess MW; Division of Histology and Embryology, Innsbruck Medical University, Innsbruck, Austria.
  • Huber LA; Division of Cell Biology, Biocenter Innsbruck, Innsbruck, Austria.
  • Stapelbroek JM; Division of Pediatrics, Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands.
  • Müller T; Department of Pediatrics I, Biocenter Innsbruck, Innsbruck, Austria. Electronic address: thomas.mueller@uki.at.
  • Middendorp S; Division of Pediatrics, Department of Pediatric Gastroenterology, Wilhelmina Children's Hospital, University Medical Center Utrecht, Utrecht, The Netherlands. Electronic address: s.middendorp@umcutrecht.nl.
Gastroenterology ; 147(1): 65-68.e10, 2014 Jul.
Article in En | MEDLINE | ID: mdl-24726755
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Full text: 1 Database: MEDLINE Main subject: Qa-SNARE Proteins / Malabsorption Syndromes / Microvilli / Mucolipidoses / Mutation Type of study: Etiology_studies Limits: Female / Humans / Infant / Male Language: En Year: 2014 Type: Article
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Full text: 1 Database: MEDLINE Main subject: Qa-SNARE Proteins / Malabsorption Syndromes / Microvilli / Mucolipidoses / Mutation Type of study: Etiology_studies Limits: Female / Humans / Infant / Male Language: En Year: 2014 Type: Article