Unusual Clinical and Molecular-Pathological Profile of Gerstmann-Sträussler-Scheinker Disease Associated With a NovelPRNPMutation (V176G)-Reference-Cited by-同舟云学术

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Unusual Clinical and Molecular-Pathological Profile of Gerstmann-Sträussler-Scheinker Disease Associated With a NovelPRNPMutation (V176G)

Published:2013-09-01 Issue:9 Volume:70 Page:1180
ISSN:2168-6149
Container-title:JAMA Neurology
language:en
Short-container-title:JAMA Neurol

Author:

Simpson Marion,Johanssen Vanessa,Boyd Alison,Klug Genevieve,Masters Colin L.,Li Qiao-Xin,Pamphlett Roger,McLean Catriona,Lewis Victoria,Collins Steven J.

Publisher

American Medical Association (AMA)

Subject

Neurology (clinical)

Cited by 18 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

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2. On the role of the cellular prion protein in the uptake and signaling of pathological aggregates in neurodegenerative diseases;Prion;2020-01-01

3. The role of the cellular prion protein in the uptake and toxic signaling of pathological neurodegenerative aggregates;Progress in Molecular Biology and Translational Science;2020

4. Atomic insights into the effects of pathological mutants through the disruption of hydrophobic core in the prion protein;Scientific Reports;2019-12

5. Age of onset in genetic prion disease and the design of preventive clinical trials;2018-08-29

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