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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Detalles Bibliográficos
Autores principales: Lin, Chin-Hsien, Chen, Ta-Fu, Chiu, Ming-Jang, Lin, Han-I, Wu, Ruey-Meei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Neuroscience
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009437/
https://www.ncbi.nlm.nih.gov/pubmed/24803912
http://dx.doi.org/10.3389/fneur.2014.00059

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4009437/
https://www.ncbi.nlm.nih.gov/pubmed/24803912
http://dx.doi.org/10.3389/fneur.2014.00059

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