A Chinese patient with the clinical features of Parkinson’s disease contains a single copy of octarepeat deletion in PRNP case report

Insertion or deletion of single copy of octapeptide repeat (OR) in human PrP protein are considered as polymorphism, while of insertions of more numbers of OR and deletion of two copies of OR are associated with genetic prion diseases. Here, we reported a 58-year-old female patient who displayed cli...

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Detalles Bibliográficos
Autores principales: Shi, Qi, Shen, Xiao-Jing, Gao, Li-Ping, Xiao, Kang, Zhou, Wei, Wang, Yuan, Chen, Cao, Dong, Xiao-Ping
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2021
Materias:
Case Reports
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259714/
https://www.ncbi.nlm.nih.gov/pubmed/34224312
http://dx.doi.org/10.1080/19336896.2021.1946376

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8259714/
https://www.ncbi.nlm.nih.gov/pubmed/34224312
http://dx.doi.org/10.1080/19336896.2021.1946376

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