首页 | 官方网站   微博 | 高级检索  
     


GRIN1 mutations cause encephalopathy with infantile‐onset epilepsy,and hyperkinetic and stereotyped movement disorders
Authors:Chihiro Ohba  Masaaki Shiina  Jun Tohyama  Kazuhiro Haginoya  Tally Lerman‐Sagie  Nobuhiko Okamoto  Lubov Blumkin  Dorit Lev  Souichi Mukaida  Fumihito Nozaki  Mitsugu Uematsu  Akira Onuma  Hirofumi Kodera  Mitsuko Nakashima  Yoshinori Tsurusaki  Noriko Miyake  Fumiaki Tanaka  Mitsuhiro Kato  Kazuhiro Ogata  Hirotomo Saitsu  Naomichi Matsumoto
Affiliation:1. Department of Human Genetics, Graduate School of Medicine, Yokohama City University, Yokohama, Japan;2. Department of Clinical Neurology and Stroke Medicine, Yokohama City University, Yokohama, Japan;3. Department of Biochemistry, Graduate School of Medicine, Yokohama City University, Yokohama, Japan;4. Department of Pediatrics, Epilepsy Center, Nishi‐Niigata Chuo National Hospital, Niigata, Japan;5. Department of Pediatric Neurology, Takuto Rehabilitation Center for Children, Sendai, Japan;6. Metabolic Neurogenetic Clinic, Wolfson Medical Center, Holon, Israel;7. Department of Medical Genetics, Osaka Medical Center, Research Institute for Maternal and Child Health, Osaka, Japan;8. Department of Pediatric Neurology, National Hospital Organization Utano Hospital, Kyoto, Japan;9. Department of Pediatrics, Shiga Medical Center for Children, Shiga, Japan;10. Department of Pediatrics, Tohoku University School of Medicine, Sendai, Japan;11. Department of Pediatrics, Ekoh‐Ryoikuen, Sendai, Japan;12. Department of Pediatrics, Faculty of Medicine, Yamagata University, Yamagata, Japan
Abstract:
Keywords:   GRIN1     Encephalopathy  Neurotransmitter disorders  Seizure  Movement disorders
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司    京ICP备09084417号-23

京公网安备 11010802026262号