Exome sequencing identifies a novel TTN mutation in a family with hereditary myopathy with early respiratory failure

Author(s)

    • SUZUKI Naoki
    • Department of Neurology, Tohoku University School of Medicine
    • KATO Masaaki
    • Department of Neurology, Tohoku University School of Medicine
    • TAKAHASHI Toshiaki
    • Department of Neurology and Division of Clinical Research, National Hospital Organization Nishitaga National Hospital
    • TATEYAMA Maki
    • Department of Neurology, Tohoku University School of Medicine
    • NAGASHIMA Takeshi
    • Division of Cell Proliferation, United Centers for Advanced Research and Translational Medicine, Tohoku University Graduate School of Medicine
    • FUNAYAMA Ryo
    • Division of Cell Proliferation, United Centers for Advanced Research and Translational Medicine, Tohoku University Graduate School of Medicine
    • ABE Koji
    • Department of Neurology, Okayama University Medical School
    • NAKAYAMA Keiko
    • Division of Cell Proliferation, United Centers for Advanced Research and Translational Medicine, Tohoku University Graduate School of Medicine
    • AOKI Masashi
    • Department of Neurology, Tohoku University School of Medicine

Journal

  • Journal of human genetics

    Journal of human genetics 58(5), 259-266, 2013-05-01

    Nature Publishing Group

References:  34

Codes

  • NII Article ID (NAID)
    10031177220
  • NII NACSIS-CAT ID (NCID)
    AA11206160
  • Text Lang
    ENG
  • Article Type
    ART
  • ISSN
    14345161
  • NDL Article ID
    024521860
  • NDL Call No.
    Z54-H248
  • Data Source
    CJP  NDL 
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