Congenital myopathy with fiber-type disproportion accompanied by dilated cardiomyopathy in a patient with a novel p.G48A ACTA1 mutation

著录项

• 来源
  《Journal of the Neurological Sciences: Official Bulletin of the World Federation of Neurology》 |2018年第2018期|共3页
• 作者

  Koh Tadokoro; Yasuyuki Ohta; Ryo Sasaki; Yoshiaki Takahashi; Kota Sato; Jingwei Shang; Mami Takemoto; Nozomi Hishikawa; Toru Yamashita; Kazufumi Nakamura; Ichizo Nishino; Koji Abe;

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• 作者单位

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

  Department of Cardiovascular Medicine Graduate School of Medicine Dentistry and Pharmaceutical;

  Department of Neuromuscular Research National Institute of Neuroscience National Center of;

  Department of Neurology Graduate School of Medicine Dentistry and Pharmaceutical Sciences;

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• 收录信息
• 原文格式 PDF
• 正文语种 eng
• 中图分类 神经病学;
• 关键词

  ACTA1; Congenital fiber-type disproportion; Dilated cardiomyopathy; p.G48A;

  机译：acta1;先天性纤维型歧化;扩张心肌病;p.g48a;