Low survival rate and muscle fiber-dependent aging effects in the McArdle disease mouse model
Author:
Funder
Ministry of Economy and Competitiveness | Instituto de Salud Carlos III
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/s41598-019-41414-8.pdf
Reference31 articles.
1. Dimauro, S., Andreu, A. L., Bruno, C. & Hadjigeorgiou, G. M. Myophosphorylase deficiency (glycogenosis type V; McArdle disease). Current molecular medicine 2, 189–196 (2002).
2. Lucia, A. et al. McArdle disease: what do neurologists need to know? Nature clinical practice. Neurology 4, 568–577, https://doi.org/10.1038/ncpneuro0913 (2008).
3. Dimauro, S., Akman, O. & Hays, A. P. Disorders of carbohydrate metabolism. Handbook of clinical neurology 86, 167–182, https://doi.org/10.1016/S0072-9752(07)86007-6 (2007).
4. Lucia, A. et al. Genotypic and phenotypic features of McArdle disease: insights from the Spanish national registry. Journal of neurology, neurosurgery, and psychiatry 83, 322–328, https://doi.org/10.1136/jnnp-2011-301593 (2012).
5. Santalla, A. et al. Genotypic and phenotypic features of all Spanish patients with McArdle disease: a 2016 update. BMC genomics 18, 819, https://doi.org/10.1186/s12864-017-4188-2 (2017).
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