Nucleocytoplasmic transport defect in a North American patient with ALS8
Author:
Affiliation:
1. Neurogenetics Branch; National Institute of Neurological Disorders and Stroke; NIH; 35 Convent Drive Bethesda Maryland 20892
2. Neuromuscular Center; Cleveland Clinic; 9500 Euclid Avenue Cleveland Ohio 44195
Funder
National Institute of Neurological Disorders and Stroke
Publisher
Wiley
Subject
Neurology (clinical),General Neuroscience
Reference24 articles.
1. Decoding ALS: from genes to mechanism;Taylor;Nature,2016
2. A mutation in the vesicle-trafficking protein VAPB causes late-onset spinal muscular atrophy and amyotrophic lateral sclerosis;Nishimura;Am J Hum Genet,2004
3. A common founder for amyotrophic lateral sclerosis type 8 (ALS8) in the Brazilian population;Nishimura;Hum Genet,2005
4. The p. P56S mutation in the VAPB gene is not due to a single founder: the first European case;Funke;Clin Genet,2010
5. Atypical familial amyotrophic lateral sclerosis with initial symptoms of pain or tremor in a Chinese family harboring VAPB-P56S mutation;Di;J Neurol,2016
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