骨格筋Na^+ channel遺伝子の点変異を認めたparamyotonia congenitaの1家系  [in Japanese] A Japanese family with paramyotonia congenita which has a mutation in the muscle sodium channel gene  [in Japanese]

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Author(s)

    • 越智 博文 OCHI Hirofumi
    • 九州大学医学部脳研神経内科 Department of neurology, Neurological Institute, Faculty of Medicine, Kyushu University
    • 山田 猛 YAMADA Takeshi
    • 九州大学医学部脳研神経内科 Department of neurology, Neurological Institute, Faculty of Medicine, Kyushu University
    • 原 英夫 HARA Hideo
    • 九州大学医学部脳研神経内科 Department of neurology, Neurological Institute, Faculty of Medicine, Kyushu University
    • 由村 健夫 YOSHIMURA Takeo
    • 九州大学医学部脳研神経内科 Department of neurology, Neurological Institute, Faculty of Medicine, Kyushu University
    • 小林 卓郎 KOBAYASHI Takuro
    • 九州大学医学部脳研神経内科 Department of neurology, Neurological Institute, Faculty of Medicine, Kyushu University

Journal

  • Rinsho Shinkeigaku (Clinical Neurol)

    Rinsho Shinkeigaku (Clinical Neurol) 35(8), 893-896, 1995-08-01

Cited by:  2

Codes

  • NII Article ID (NAID)
    10008313861
  • NII NACSIS-CAT ID (NCID)
    AN00253207
  • Text Lang
    JPN
  • Article Type
    Journal Article
  • ISSN
    0009918X
  • Data Source
    CJP  CJPref 
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