Limb-girdle muscular dystrophies — international collaborations for translational research
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Clinical Neurology
Link
http://www.nature.com/articles/nrneurol.2016.35.pdf
Reference82 articles.
1. Walton, J. N. & Nattrass, F. J. On the classification, natural history and treatment of the myopathies. Brain 77, 169–231 (1954).
2. Fanin, M., Nascimbeni, A. C., Fulizio, L. & Angelini, C. The frequency of limb girdle muscular dystrophy 2A in northeastern Italy. Neuromuscul. Disord. 15, 218–224 (2005).
3. Narayanaswami, P. et al. Evidence-based guideline summary: diagnosis and treatment of limb-girdle and distal dystrophies: report of the Guideline Development Subcommittee of the American Academy of Neurology and the Practice Issues Review Panel of the American Association of Neuromuscular and Electrodiagnostic Medicine. Neurology 83, 1453–1463 (2014).
4. Nigro, V. & Savarese, M. Genetic basis of limb-girdle muscular dystrophies: the 2014 update. Acta Myol. 33, 1–12 (2014).
5. Murphy, A. P. & Straub, V. The classification, natural history and treatment of the limb girdle muscular dystrophies. J. Neuromuscul. Dis. 2 (Suppl. 2), 7–19 (2015).
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