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Biallelic COLGALT1 variants are associated with cerebral small vessel disease.
Miyatake, Satoko; Schneeberger, Sacha; Koyama, Norihisa; Yokochi, Kenji; Ohmura, Kayo; Shiina, Masaaki; Mori, Harushi; Koshimizu, Eriko; Imagawa, Eri; Uchiyama, Yuri; Mitsuhashi, Satomi; Frith, Martin C; Fujita, Atsushi; Satoh, Mai; Taguri, Masataka; Tomono, Yasuko; Takahashi, Keita; Doi, Hiroshi; Takeuchi, Hideyuki; Nakashima, Mitsuko; Mizuguchi, Takeshi; Takata, Atsushi; Miyake, Noriko; Saitsu, Hirotomo; Tanaka, Fumiaki; Ogata, Kazuhiro; Hennet, Thierry; Matsumoto, Naomichi.
Afiliación
  • Miyatake S; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Schneeberger S; Clinical Genetics Department, Yokohama City University Hospital, Yokohama, Japan.
  • Koyama N; Institute of Physiology, University of Zurich, Zurich, Switzerland.
  • Yokochi K; Department of Pediatrics, Toyohashi Municipal Hospital, Toyohashi, Japan.
  • Ohmura K; Department of Pediatrics, Toyohashi Municipal Hospital, Toyohashi, Japan.
  • Shiina M; Department of Pediatrics, Seirei Mikatahara General Hospital, Shizuoka, Japan.
  • Mori H; Department of Pediatric Neurology, Morinomiya Hospital, Osaka, Japan.
  • Koshimizu E; Department of Biochemistry, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Imagawa E; Department of Radiology, Graduate School and Faculty of Medicine, University of Tokyo, Tokyo, Japan.
  • Uchiyama Y; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Mitsuhashi S; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Frith MC; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Fujita A; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Satoh M; Artificial Intelligence Research Center, National Institute of Advanced Industrial Science and Technology, Tokyo, Japan.
  • Taguri M; Graduate School of Frontier Sciences, University of Tokyo, Chiba, Japan.
  • Tomono Y; Computational Bio Big-Data Open Innovation Laboratory, National Institute of Advanced Industrial Science and Technology, Tokyo, Japan.
  • Takahashi K; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Doi H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Takeuchi H; Department of Data Science, Yokohama City University School of Data Science, Yokohama, Japan.
  • Nakashima M; Division of Molecular and Cell Biology, Shigei Medical Research Institute, Okayama, Japan.
  • Mizuguchi T; Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Takata A; Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Miyake N; Department of Neurology and Stroke Medicine, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Saitsu H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Tanaka F; Department of Biochemistry, Hamamatsu University School of Medicine, Shizuoka, Japan.
  • Ogata K; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Hennet T; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
Ann Neurol ; 84(6): 843-853, 2018 12.
Article en En | MEDLINE | ID: mdl-30412317
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Colágeno Tipo IV / Enfermedades de los Pequeños Vasos Cerebrales / Mutación Tipo de estudio: Risk_factors_studies Límite: Child / Humans / Male Idioma: En Revista: Ann Neurol Año: 2018 Tipo del documento: Article País de afiliación: Japón
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Predisposición Genética a la Enfermedad / Colágeno Tipo IV / Enfermedades de los Pequeños Vasos Cerebrales / Mutación Tipo de estudio: Risk_factors_studies Límite: Child / Humans / Male Idioma: En Revista: Ann Neurol Año: 2018 Tipo del documento: Article País de afiliación: Japón