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

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...

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Bibliographic Details
Main Authors: 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.
Other Authors: Lee Kong Chian School of Medicine (LKCMedicine)
Format: Journal Article
Language:English
Published: 2023
Subjects:
Science::Medicine
Alzheimer Disease
Amyotrophic Lateral Sclerosis
Online Access:https://hdl.handle.net/10356/169821

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