Accumulation Area of a Japanese <i>PRNP</i> P102L Variant Associated With Gerstmann-Sträussler-Scheinker Disease: The Ariake <i>PRNP</i> P102L Variant-Reference-Cited by-同舟云学术

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Accumulation Area of a Japanese PRNP P102L Variant Associated With Gerstmann-Sträussler-Scheinker Disease: The Ariake PRNP P102L Variant

Published:2024 Issue:3 Volume:20 Page:321
ISSN:1738-6586
Container-title:Journal of Clinical Neurology
language:en
Short-container-title:J Clin Neurol

Author:

Suzuyama Kohei¹^ORCID,Eriguchi Makoto¹^ORCID,Minagawa Hiromu¹,Honda Hiroyuki²³^ORCID,Kai Keita⁴^ORCID,Kitamoto Tetsuyuki⁵^ORCID,Hara Hideo¹^ORCID

Affiliation:

1. Division of Neurology, Department of Internal Medicine, Saga University Faculty of Medicine, Saga, Japan.

2. Department of Neuropathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

3. Department of Neurology, Neuro Muscular Center, National Hospital Organization Omuta National Hospital, Omuta, Japan.

4. Department of Pathology, Saga University Hospital, Saga, Japan.

5. Department of Neurological Science, Tohoku University Graduate School of Medicine, Sendai, Japan.

Publisher

XMLink

Link

https://thejcn.com/pdf/10.3988/jcn.2023.0102

Reference35 articles.

1. Genetic PrP Prion Diseases

2. Linkage of a prion protein missense variant to Gerstmann–Sträussler syndrome

3. A new inherited prion disease (PrP-P105L mutation) showing spastic paraparesis

4. Inherited prion disease with A117V mutation of the prion protein gene: a novel Hungarian family

5. Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Involvement of the nigrostriatal system in Gerstman–Sträussler–Scheinker disease with the PRNP-P102L mutation;Journal of the Neurological Sciences;2024-09

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