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

Yi Jayne Tan,Alisa C W Yong,Jia Nee Foo,Michelle M Lian,Weng Khong Lim,Jacqueline Dominguez,Zhi Hui Fong,Kaavya Narasimhalu,Hui Jin Chiew,Kok Pin Ng,Simon K S Ting,Nagaendran Kandiah,Adeline S L Ng

Annals of clinical and translational neurology（2023）

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摘要

In our cohort, genetic mutations are present in one-quarter of FTD-spectrum cases, and up to half of those with family history. Our findings highlight the importance of wider implementation of genetic testing in FTD patients from Southeast Asia.

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关键词

genetic frontotemporal dementia,frontotemporal dementia,common cause

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