A Systematic and Comprehensive Review on Disease-Causing Genes in Amyotrophic Lateral Sclerosis
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,General Medicine
Link
https://link.springer.com/content/pdf/10.1007/s12031-020-01569-w.pdf
Reference170 articles.
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2. Acharya V, Nagarajaram HA (2012) Hansa: an automated method for discriminating disease and neutral human nsSNPs. Hum Mutat 33:332–337. https://doi.org/10.1002/humu.21642
3. Ajroud-Driss S, Siddique T (2015) Sporadic and hereditary amyotrophic lateral sclerosis (ALS). Biochim Biophys Acta (BBA) - Mol Basis Dis 1852:679–684. https://doi.org/10.1016/j.bbadis.2014.08.010
4. Alami NH, Smith RB, Carrasco MA et al (2014) Axonal transport of TDP-43 mRNA granules is impaired by ALS-causing mutations. Neuron 81:536–543. https://doi.org/10.1016/j.neuron.2013.12.018
5. Al-Chalabi A, Jones A, Troakes C et al (2012) The genetics and neuropathology of amyotrophic lateral sclerosis. Acta Neuropathol (Berl) 124:339–352. https://doi.org/10.1007/s00401-012-1022-4
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