FTD-PSP is an Unusual Clinical Phenotype in A Frontotemporal Dementia Patient with A Novel Progranulin Mutation

Progranulin (GRN) mutations are a major cause of frontotemporal dementia (FTD); the spectrum of clinical phenotypes of FTD is much more extensive than previously reported. The frequency and locations of GRN mutations in Chinese patients with FTD remain uncertain. We performed cDNA sequencing in one...

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Detalles Bibliográficos
Autores principales: Deng, Bin, Zheng, Zhe, Zheng, Jialing, Yang, Wanlin, Huang, Yu, Luo, Yuqi, Jin, Dana, Shen, Lu, Jin, Kunlin, Wang, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: JKL International LLC 2021
Materias:
Orginal Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460311/
https://www.ncbi.nlm.nih.gov/pubmed/34631218
http://dx.doi.org/10.14336/AD.2021.0309

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8460311/
https://www.ncbi.nlm.nih.gov/pubmed/34631218
http://dx.doi.org/10.14336/AD.2021.0309

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