Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene-Reference-Cited by-同舟云学术

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Creutzfeldt-Jakob disease with a novel extra-repeat insertional mutation in the PRNP gene

Published:2003-11-10 Issue:9 Volume:61 Page:1288-1291
ISSN:0028-3878
Container-title:Neurology
language:en
Short-container-title:Neurology

Author:

Pietrini V.,Puoti G.,Limido L.,Rossi G.,Di Fede G.,Giaccone G.,Mangieri M.,Tedeschi F.,Bondavalli A.,Mancia D.,Bugiani O.,Tagliavini F.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Neurology (clinical)

Cited by 25 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. SORL1 gene mutation and octapeptide repeat insertion in PRNP gene in a case presenting with rapidly progressive dementia and cerebral amyloid angiopathy;European Journal of Neurology;2022-07-22

2. Inherited Creutzfeldt–Jakob disease with four-octapeptide repeat insertional mutation in the prion gene;Rinsho Shinkeigaku;2021

3. Characterization of Anchorless Human PrP With Q227X Stop Mutation Linked to Gerstmann-Sträussler-Scheinker Syndrome In Vivo and In Vitro;Molecular Neurobiology;2020-09-05

4. Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion;Frontiers in Cellular Neuroscience;2020-07-08

5. A case report of genetic prion disease with two different PRNP variants;Molecular Genetics & Genomic Medicine;2020-01-17

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