Lack of C9orf72 Repeat Expansion in Taiwanese Patients with Mixed Neurodegenerative Disorders

Background: The hexanucleotide repeat expansion in intron 1 of the C9orf72 gene is recognized as the most common genetic cause of frontotemporal dementia (FTD). There are overlapping clinical and pathological characteristics between FTD and Parkinsonism syndrome, and some FTD patients may present wi...

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Bibliografiske detaljer
Main Authors: Lin, Chin-Hsien, Chen, Ta-Fu, Chiu, Ming-Jang, Lin, Han-I, Wu, Ruey-Meei
Format: Artigo
Sprog:Inglês
Udgivet: Frontiers Media S.A. 2014
Fag:
Neuroscience
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4009437/
https://ncbi.nlm.nih.gov/pubmed/24803912
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fneur.2014.00059
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