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Comparative Label-Free Mass Spectrometric Analysis of Mildly versus Severely Affected mdx Mouse Skeletal Muscles Identifies Annexin, Lamin, and Vimentin as Universal Dystrophic Markers
Open AccessEditorial

Special Issue—Towards Understanding the Mechanisms and Curing of Muscular Dystrophy Diseases

The Cyprus Institute of Neurology & Genetics, PO Box 23462, 1683 Nicosia, Cyprus
Academic Editor: Derek J. McPhee
Molecules 2015, 20(7), 12944-12945; https://doi.org/10.3390/molecules200712944
Received: 14 July 2015 / Accepted: 16 July 2015 / Published: 16 July 2015
Muscular dystrophies are a heterogeneous group of inherited diseases with different molecular basss, but sharing similar clinical features and dystrophic changes. View Full-Text
MDPI and ACS Style

Phylactou, L.A. Special Issue—Towards Understanding the Mechanisms and Curing of Muscular Dystrophy Diseases. Molecules 2015, 20, 12944-12945.

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