C9orf72 expansions are the most common cause of genetic frontotemporal dementia in a Southeast Asian cohort

OBJECTIVE: Frontotemporal dementia (FTD) encompasses a spectrum of neurodegenerative disorders, including behavioural variant FTD (bvFTD), semantic variant primary progressive aphasia (svPPA) and non‐fluent variant PPA (nfvPPA). While a strong genetic component is implicated in FTD, genetic FTD in A...

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Detalles Bibliográficos
Autores principales: Tan, Yi Jayne, Yong, Alisa C. W., Foo, Jia Nee, Lian, Michelle M., Lim, Weng Khong, Dominguez, Jacqueline, Fong, Zhi Hui, Narasimhalu, Kaavya, Chiew, Hui Jin, Ng, Kok Pin, Ting, Simon K. S., Kandiah, Nagaendran, Ng, Adeline S. L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Research Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10109321/
https://www.ncbi.nlm.nih.gov/pubmed/36799407
http://dx.doi.org/10.1002/acn3.51744

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10109321/
https://www.ncbi.nlm.nih.gov/pubmed/36799407
http://dx.doi.org/10.1002/acn3.51744

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