Genetic screening in sporadic ALS and FTD

The increasing complexity of the genetic landscape in amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) presents a significant resource and physician training challenge. At least 10% of those diagnosed with ALS or FTD are known to carry an autosomal dominant genetic mutation. The...

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Dettagli Bibliografici
Pubblicato in:J Neurol Neurosurg Psychiatry
Autori principali: Turner, Martin R, Al-Chalabi, Ammar, Chio, Adriano, Hardiman, Orla, Kiernan, Matthew C, Rohrer, Jonathan D, Rowe, James, Seeley, William, Talbot, Kevin
Natura: Artigo
Lingua:Inglês
Pubblicazione: BMJ Publishing Group 2017
Soggetti:
Neurodegeneration
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5740553/
https://ncbi.nlm.nih.gov/pubmed/28642287
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jnnp-2017-315995
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