Detection of a novel frameshift mutation and regions with homozygosis within ARHGEF28 gene in familial amyotrophic lateral sclerosis
Author:
Publisher
Informa UK Limited
Subject
Clinical Neurology,Neurology
Link
http://www.tandfonline.com/doi/pdf/10.3109/21678421.2012.758288
Reference56 articles.
1. The Pathobiology of Amyotrophic Lateral Sclerosis: A Proteinopathy?
2. Amyotrophic Lateral Ssclerosis and Structural Defects in Cu,Zn Superoxide Dismutase
3. Mutations in Cu/Zn superoxide dismutase gene are associated with familial amyotrophic lateral sclerosis
4. TARDBP mutations in individuals with sporadic and familial amyotrophic lateral sclerosis
5. TDP-43 Mutations in Familial and Sporadic Amyotrophic Lateral Sclerosis
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