A case of hereditary motor and sensory neuropathy type I with a new type of peripheral myelin protein (PMP)-22 mutation

• OHNISHI Akio

  Department of Neurology, University of Occupational and Environmental Health

• YOSHIMURA Takeo

  Department of Neurology, Neurological Institute, Faculty of Medicine, Kyushu University

• KANEHISA Yoshihide

  Department of Internal Medicine, Kure Mutual Hospital

• FUKUSHIMA Yoshimitsu

  Division of Medical Genetics, Saitama Children's Medical Center

Bibliographic Information

Other Title

• Peripheral myelin protein (PMP)-22遺伝子の新しい型の変異を示す遺伝性運動感覚性ニューロパチー タイプIの1例

Journal

• 臨床神経学

  臨床神経学 35 (7), 788-792, 1995-07-01

Keywords

• Charcot-Marie-Tooth disease
• hereditary motor and sensory neuropathy
• HMSN type I
• peripheral myelin protein (PMP)-22
• point mutation

Details

• CRID: 1572824499541796224
• NII Article ID: 10008313532
• NII Book ID: AN00253207
• ISSN: 0009918X
• Web Site: https://search.jamas.or.jp/link/ui/1996077315
• Text Lang: ja
• Data Source:
  • CiNii Articles