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Congenital fiber type disproportion myopathy caused by LMNA mutations.
Kajino, Sachiko; Ishihara, Kayo; Goto, Kanako; Ishigaki, Keiko; Noguchi, Satoru; Nonaka, Ikuya; Osawa, Makiko; Nishino, Ichizo; Hayashi, Yukiko K.
Afiliação
  • Kajino S; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Ishihara K; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Goto K; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Ishigaki K; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Noguchi S; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan; Department of Clinical Development, Translational Medical Center, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Nonaka I; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Osawa M; Department of Pediatrics, Tokyo Women's Medical University, School of Medicine, Tokyo, Japan.
  • Nishino I; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan; Department of Clinical Development, Translational Medical Center, National Center of Neurology and Psychiatry, Tokyo, Japan.
  • Hayashi YK; Department of Neuromuscular Research, National Institute of Neuroscience, National Center of Neurology and Psychiatry, Tokyo, Japan; Department of Clinical Development, Translational Medical Center, National Center of Neurology and Psychiatry, Tokyo, Japan; Department of Neurophysiology, Tokyo Medic
J Neurol Sci ; 340(1-2): 94-8, 2014 May 15.
Article em En | MEDLINE | ID: mdl-24642510
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deleção de Sequência / Miopatias Congênitas Estruturais / Lamina Tipo A Idioma: En Ano de publicação: 2014 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Deleção de Sequência / Miopatias Congênitas Estruturais / Lamina Tipo A Idioma: En Ano de publicação: 2014 Tipo de documento: Article