The Spectrum of C9orf72-mediated Neurodegeneration and Amyotrophic Lateral Sclerosis

The discovery that a hexanucleotide repeat expansion in C9orf72 is the most numerous genetic variant of both amyotrophic lateral sclerosis and frontotemporal dementia has opened a rapidly growing field, which may provide long hoped for advances in the understanding and treatment of these devastating...

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Detalles Bibliográficos
Autores principales: Cooper-Knock, Johnathan, Kirby, Janine, Highley, Robin, Shaw, Pamela J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2015
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404438/
https://www.ncbi.nlm.nih.gov/pubmed/25731823
http://dx.doi.org/10.1007/s13311-015-0342-1

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4404438/
https://www.ncbi.nlm.nih.gov/pubmed/25731823
http://dx.doi.org/10.1007/s13311-015-0342-1

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