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SLITRK2 variants associated with neurodevelopmental disorders impair excitatory synaptic function and cognition in mice.
El Chehadeh, Salima; Han, Kyung Ah; Kim, Dongwook; Jang, Gyubin; Bakhtiari, Somayeh; Lim, Dongseok; Kim, Hee Young; Kim, Jinhu; Kim, Hyeonho; Wynn, Julia; Chung, Wendy K; Vitiello, Giuseppina; Cutcutache, Ioana; Page, Matthew; Gecz, Jozef; Harper, Kelly; Han, Ah-Reum; Kim, Ho Min; Wessels, Marja; Bayat, Allan; Jaén, Alberto Fernández; Selicorni, Angelo; Maitz, Silvia; de Brouwer, Arjan P M; Silfhout, Anneke Vulto-van; Armstrong, Martin; Symonds, Joseph; Küry, Sébastien; Isidor, Bertrand; Cogné, Benjamin; Nizon, Mathilde; Feger, Claire; Muller, Jean; Torti, Erin; Grange, Dorothy K; Willems, Marjolaine; Kruer, Michael C; Ko, Jaewon; Piton, Amélie; Um, Ji Won.
Afiliación
  • El Chehadeh S; Service de Génétique Médicale, Institut de Génétique Médicale d'Alsace (IGMA), Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
  • Han KA; Institut de Génétique et de Biologie Moléculaire et Cellulaire (IGBMC), INSERM U1258, CNRS-UMR7104, Université de Strasbourg, Illkirch-Graffenstaden, France.
  • Kim D; Laboratoire de Génétique Médicale, UMRS_1112, Institut de Génétique Médicale d'Alsace (IGMA), Université de Strasbourg et INSERM, Strasbourg, France.
  • Jang G; Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Korea.
  • Bakhtiari S; Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Korea.
  • Lim D; Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Korea.
  • Kim HY; Pediatric Movement Disorders Program, Division of Pediatric Neurology, Barrow Neurological Institute, Phoenix Children's Hospital, Phoenix, AZ, USA.
  • Kim J; Departments of Child Health, Neurology, Cellular & Molecular Medicine and Program in Genetics, University of Arizona College of Medicine, Phoenix, AZ, USA.
  • Kim H; Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Korea.
  • Wynn J; Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Korea.
  • Chung WK; Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Korea.
  • Vitiello G; Department of Brain Sciences, Daegu Gyeongbuk Institute of Science and Technology (DGIST), Daegu, 42988, Korea.
  • Cutcutache I; Departments of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Page M; Departments of Pediatrics, Columbia University Medical Center, New York, NY, USA.
  • Gecz J; Department of Medicine, Columbia University, New York, NY, 10032, USA.
  • Harper K; Department of Molecular Medicine and Medical Biotechnologies, Federico II University Hospital, Via Pansini 5, 80131, Naples, Italy.
  • Han AR; Translational Medicine, UCB Pharma, Slough, UK.
  • Kim HM; Translational Medicine, UCB Pharma, Slough, UK.
  • Wessels M; Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia.
  • Bayat A; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • Jaén AF; Women and Kids, South Australian Health and Medical Research Institute, Adelaide, South Australia, Australia.
  • Selicorni A; Adelaide Medical School, Faculty of Health and Medical Sciences, The University of Adelaide, Adelaide, South Australia, Australia.
  • Maitz S; Robinson Research Institute, The University of Adelaide, Adelaide, South Australia, Australia.
  • de Brouwer APM; Center for Biomolecular and Cellular Structure, Institute for Basic Science, Daejeon, 34126, Korea.
  • Silfhout AV; Center for Biomolecular and Cellular Structure, Institute for Basic Science, Daejeon, 34126, Korea.
  • Armstrong M; Graduate School of Medical Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), Daejeon, 34141, Korea.
  • Symonds J; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, The Netherlands.
  • Küry S; Department of Epilepsy Genetics and Personalized Medicine, Danish Epilepsy Center, Dianalund, Denmark.
  • Isidor B; Institute for Regional Health Services, University of Southern Denmark, Odense, Denmark.
  • Cogné B; Department of Pediatrics Neurology, Quirónsalud Hospital & Universidad Europea, Madrid, Spain.
  • Nizon M; Department of Pediatrics, Center for Fragile Child, ASST Lariana Sant'Anna Hospital, San Fermo della Battaglia, Como, Italy.
  • Feger C; Fondazione MBBM, Monza, Italy.
  • Muller J; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Torti E; Department of Human Genetics, Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands.
  • Grange DK; Department of Clinical Genetics, Maastricht University Medical Centre, Maastricht, The Netherlands.
  • Willems M; Translational Medicine, UCB Pharma, Braine-l'Alleud, Belgium.
  • Kruer MC; Paediatric Neurosciences Research Group, Royal Hospital for Children, Queen Elizabeth University Hospitals, Glasgow, UK.
  • Ko J; Service de Génétique Médicale, CHU Nantes, Nantes, France.
  • Piton A; Nantes Université, CNRS, INSERM, l'institut du thorax, F-44000, Nantes, France.
  • Um JW; Service de Génétique Médicale, CHU Nantes, Nantes, France.
Nat Commun ; 13(1): 4112, 2022 07 15.
Article en En | MEDLINE | ID: mdl-35840571
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sinapsis / Trastornos del Neurodesarrollo Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2022 Tipo del documento: Article País de afiliación: Francia
Texto completo
Imprimir
XML
PubMed Links
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Sinapsis / Trastornos del Neurodesarrollo Tipo de estudio: Risk_factors_studies Límite: Animals Idioma: En Revista: Nat Commun Asunto de la revista: BIOLOGIA / CIENCIA Año: 2022 Tipo del documento: Article País de afiliación: Francia