A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
Kazumichi Ota,
Yoshihiko Nakazato,
Ryu Yokoyama,
Hitoshi Kawasaki,
Naotoshi Tamura,
Akira Ohtake,
Megumi Saito-Tsuruoka,
Toshimasa Yamamoto
Affiliations
Kazumichi Ota
Department of Neurology, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan; Corresponding author at: Department of Neurology, Saitama Medical School, 38 Morohongo Moroyama, Iruma-gun, Saitama 350-0495, Japan.
Yoshihiko Nakazato
Department of Neurology, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan
Ryu Yokoyama
Department of Neurology, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan
Hitoshi Kawasaki
Department of Neurology, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan
Naotoshi Tamura
Department of Neurology, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan
Akira Ohtake
Department of Clinical Genomics, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan; Center for Intractable Diseases, Saitama Medical University Hospital, Saitama 350-0495, Japan
Megumi Saito-Tsuruoka
Department of Clinical Genomics, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan; Center for Intractable Diseases, Saitama Medical University Hospital, Saitama 350-0495, Japan
Toshimasa Yamamoto
Department of Neurology, Faculty of Medicine, Saitama Medical University, Saitama 350-0495, Japan
