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M Laurá

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Neuromuscular Disorders : NMD|January 4, 2011
Variable phenotypes are associated with PMP22 missense mutationsM Russo, M Laurá, J M Polke, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, 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.
Pageof 1

Showing results (1-10 of 3) with videos related to

Sort By:
Pageof 1
Neuromuscular Disorders : NMD|January 4, 2011
Variable phenotypes are associated with PMP22 missense mutationsM Russo, M Laurá, J M Polke, et al.
Neurology|July 1, 2011
Recessive axonal Charcot-Marie-Tooth disease due to compound heterozygous mitofusin 2 mutationsJ M Polke, M Laurá, D Pareyson, 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.
Pageof 1