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ATP1A3 variants and slowly progressive cerebellar ataxia without paroxysmal or episodic symptoms in children.
Sasaki, Masayuki; Sumitomo, Noriko; Shimizu-Motohashi, Yuko; Takeshita, Eri; Kurosawa, Kenji; Kosaki, Kenjiro; Iwama, Kazuhiro; Mizuguchi, Takeshi; Matsumoto, Naomichi.
Affiliation
  • Sasaki M; Department of Child Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Sumitomo N; Department of Child Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Shimizu-Motohashi Y; Department of Child Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Takeshita E; Department of Child Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Kurosawa K; Division of Genetics, Kanagawa Children's Medical Center, Yokohama, Japan.
  • Kosaki K; Center for Medical Genetics, Keio University School of Medicine, Tokyo, Japan.
  • Iwama K; Department of Human Genetics, Yokohama City University Graduate School of Medicine, 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.
Dev Med Child Neurol ; 63(1): 111-115, 2021 01.
Article in En | MEDLINE | ID: mdl-32895939
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebellar Ataxia / Sodium-Potassium-Exchanging ATPase Type of study: Diagnostic_studies Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Dev Med Child Neurol Year: 2021 Type: Article Affiliation country: Japan
Fulltext
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PubMed Links
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cerebellar Ataxia / Sodium-Potassium-Exchanging ATPase Type of study: Diagnostic_studies Limits: Adolescent / Child / Female / Humans / Male Language: En Journal: Dev Med Child Neurol Year: 2021 Type: Article Affiliation country: Japan