Comparative analysis of C9orf72 and sporadic disease in an ALS clinic population

OBJECTIVE: We investigated whether the C9orf72 expansion mutation in patients with amyotrophic lateral sclerosis (ALS) is associated with unique demographic and clinical features. METHODS: Between 2001 and 2015, approximately half of all patients attending the Emory ALS Clinic agreed to donate DNA f...

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Pubblicato in:Neurology
Autori principali: Umoh, Mfon E., Fournier, Christina, Li, Yingjie, Polak, Meraida, Shaw, Latoya, Landers, John E., Hu, William, Gearing, Marla, Glass, Jonathan D.
Natura: Artigo
Lingua:Inglês
Pubblicazione: Lippincott Williams & Wilkins 2016
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Article
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC5027809/
https://ncbi.nlm.nih.gov/pubmed/27488601
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1212/WNL.0000000000003067
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