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A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report

Detalles Bibliográficos
Autores principales: Ota, Kazumichi, Nakazato, Yoshihiko, Yokoyama, Ryu, Kawasaki, Hitoshi, Tamura, Naotoshi, Ohtake, Akira, Saito-Tsuruoka, Megumi, Yamamoto, Toshimasa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607161/
https://www.ncbi.nlm.nih.gov/pubmed/34841096
http://dx.doi.org/10.1016/j.ensci.2021.100380
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author Ota, Kazumichi
Nakazato, Yoshihiko
Yokoyama, Ryu
Kawasaki, Hitoshi
Tamura, Naotoshi
Ohtake, Akira
Saito-Tsuruoka, Megumi
Yamamoto, Toshimasa
author_facet Ota, Kazumichi
Nakazato, Yoshihiko
Yokoyama, Ryu
Kawasaki, Hitoshi
Tamura, Naotoshi
Ohtake, Akira
Saito-Tsuruoka, Megumi
Yamamoto, Toshimasa
author_sort Ota, Kazumichi
collection PubMed
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spelling pubmed-86071612021-11-26 A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report Ota, Kazumichi Nakazato, Yoshihiko Yokoyama, Ryu Kawasaki, Hitoshi Tamura, Naotoshi Ohtake, Akira Saito-Tsuruoka, Megumi Yamamoto, Toshimasa eNeurologicalSci Letters to the Editor Elsevier 2021-11-16 /pmc/articles/PMC8607161/ /pubmed/34841096 http://dx.doi.org/10.1016/j.ensci.2021.100380 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Letters to the Editor
Ota, Kazumichi
Nakazato, Yoshihiko
Yokoyama, Ryu
Kawasaki, Hitoshi
Tamura, Naotoshi
Ohtake, Akira
Saito-Tsuruoka, Megumi
Yamamoto, Toshimasa
A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
title A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
title_full A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
title_fullStr A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
title_full_unstemmed A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
title_short A Japanese family with P102L Gerstmann–Sträussler–Scheinker disease with a variant Creutzfeldt-Jakob disease-like phenotype among the siblings: A case report
title_sort japanese family with p102l gerstmann–sträussler–scheinker disease with a variant creutzfeldt-jakob disease-like phenotype among the siblings: a case report
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8607161/
https://www.ncbi.nlm.nih.gov/pubmed/34841096
http://dx.doi.org/10.1016/j.ensci.2021.100380
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