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Gait disturbance in a patient with de novo 1.0-kb SOX2 microdeletion.
Yamada, Hiroyuki; Okanishi, Tohru; Okazaki, Tetsuya; Oguri, Masayoshi; Fukuda, Hiromi; Uchiyama, Yuri; Mizuguchi, Takeshi; Matsumoto, Naomichi; Maegaki, Yoshihiro.
Affiliation
  • Yamada H; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan. Electronic address: jms433b@hotmail.com.
  • Okanishi T; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan.
  • Okazaki T; Division of Clinical Genetics, Tottori University Hospital, Yonago, Japan.
  • Oguri M; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan; Department of Medical Technology, Kagawa Prefectural University of Health Sciences, Takamatsu, Japan.
  • Fukuda H; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan.
  • Uchiyama Y; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Yokohama, Japan; Department of Rare Disease Genomics, Yokohama City University Hospital, Yokohama, Japan.
  • Mizuguchi 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.
  • Maegaki Y; Division of Child Neurology, Department of Brain and Neurosciences, Faculty of Medicine, Tottori University, Yonago, Japan.
Brain Dev ; 44(1): 68-72, 2022 Jan.
Article in En | MEDLINE | ID: mdl-34332824
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gait Disorders, Neurologic / Dystonia / SOXB1 Transcription Factors / Movement Disorders Limits: Child / Humans / Male Language: En Journal: Brain Dev Year: 2022 Document type: Article Country of publication:
Fulltext
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gait Disorders, Neurologic / Dystonia / SOXB1 Transcription Factors / Movement Disorders Limits: Child / Humans / Male Language: En Journal: Brain Dev Year: 2022 Document type: Article Country of publication: