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Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology|November 24, 2011
Strategy for genetic testing in Charcot-Marie-diseaseL J Miller, A S D Saporta, S L Sottile, et al.
Neurology|April 22, 2011
MFN2 mutations cause severe phenotypes in most patients with CMT2AS M E Feely, M Laura, C E Siskind, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|November 29, 2014
CMT subtypes and disease burden in patients enrolled in the Inherited Neuropathies Consortium natural history study: a cross-sectional analysisV Fridman, B Bundy, M M Reilly, et al.
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