SOD1A4V-mediated ALS: Absence of a closely linked modifier gene and origination in Asia
Author:
Publisher
Elsevier BV
Subject
General Neuroscience
Reference21 articles.
1. A4T mutation in the SOD1 gene causing familial amyotrophic lateral sclerosis;Aksoy;Neuroepidemiology,2003
2. Basic local alignment search tool;Altschul;J. Mol. Biol.,1990
3. Phenotypic heterogeneity in motor neuron disease patients with CuZn-superoxide dismutase mutations in Scandinavia;Andersen;Brain,1997
4. Sixteen novel mutations in the Cu/Zn superoxide dismutase gene in amyotrophic lateral sclerosis: a decade of discoveries, defects and disputes;Andersen;Amyotroph. Lateral Scler. Other Motor Neuron Disord.,2003
5. Haploview: analysis and visualization of LD and haplotype maps;Barrett;Bioinformatics,2005
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