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A Japanese family with primary familial brain calcification presenting with paroxysmal kinesigenic dyskinesia - A comprehensive mutational analysis.
Mitsutake, Akihiko; Matsukawa, Takashi; Porto, Kristine Joyce L; Sato, Tatsuya; Katsumata, Junko; Seki, Tomonari; Maekawa, Risa; Hideyama, Takuto; Tanaka, Masaki; Ishiura, Hiroyuki; Toda, Tatsushi; Tsuji, Shoji; Shiio, Yasushi.
Affiliation
  • Mitsutake A; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan. Electronic address: mitsutake-tky@umin.ac.jp.
  • Matsukawa T; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Porto KJL; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Sato T; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan.
  • Katsumata J; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan.
  • Seki T; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan.
  • Maekawa R; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan.
  • Hideyama T; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan.
  • Tanaka M; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; Institute of Medical Genomics, International University of Health and Welfare, Chiba, Japan.
  • Ishiura H; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Toda T; Department of Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.
  • Tsuji S; Department of Molecular Neurology, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan; Institute of Medical Genomics, International University of Health and Welfare, Chiba, Japan.
  • Shiio Y; Department of Neurology, Tokyo Teishin Hospital, Tokyo, Japan.
J Neurol Sci ; 418: 117091, 2020 11 15.
Article in En | MEDLINE | ID: mdl-32798841
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Basal Ganglia Diseases / Dystonia Limits: Humans Country/Region as subject: Asia Language: En Journal: J Neurol Sci Year: 2020 Document type: Article Country of publication:
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Basal Ganglia Diseases / Dystonia Limits: Humans Country/Region as subject: Asia Language: En Journal: J Neurol Sci Year: 2020 Document type: Article Country of publication: