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The Persistent Generalized Muscle Contraction in Siblings with Molybdenum Cofactor Deficiency Type A.
Yoshimura, Ayumi; Kibe, Tetsuya; Hasegawa, Hiroshi; Ichida, Kimiyoshi; Koshimizu, Eriko; Miyatake, Satoko; Matsumoto, Naomichi; Yokochi, Kenji.
Affiliation
  • Yoshimura A; Departments of Pediatrics, Seirei-Mikatahara General Hospital, Shizuoka, Japan.
  • Kibe T; Departments of Pediatrics, Seirei-Mikatahara General Hospital, Shizuoka, Japan.
  • Hasegawa H; Department of Pathophysiology, Tokyo University of Pharmacy and Life Science, Tokyo, Japan.
  • Ichida K; Department of Pathophysiology, Tokyo University of Pharmacy and Life Science, Tokyo, Japan.
  • Koshimizu E; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
  • Miyatake S; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
  • Matsumoto N; Department of Human Genetics, Yokohama City University Graduate School of Medicine, Kanagawa, Japan.
  • Yokochi K; Departments of Pediatrics, Seirei-Mikatahara General Hospital, Shizuoka, Japan.
Neuropediatrics ; 50(2): 126-129, 2019 04.
Article in En | MEDLINE | ID: mdl-30695801
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Siblings / Metal Metabolism, Inborn Errors / Muscle Contraction Type of study: Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Neuropediatrics Year: 2019 Document type: Article Affiliation country: Japón
Fulltext
Add to My VHL
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Siblings / Metal Metabolism, Inborn Errors / Muscle Contraction Type of study: Prognostic_studies Limits: Adult / Female / Humans Language: En Journal: Neuropediatrics Year: 2019 Document type: Article Affiliation country: Japón