Quantitative proteomic analysis of skeletal muscles from wild type and transgenic mice carrying recessive Ryr1 mutations linked to congenital myopathies
J. Eckhardt, A. Ruiz, S. Koenig, M. Frieden, A. Schmidt, S. Treves, F. Zorzato
The paper quantitatively analyzes proteomic differences in skeletal muscles of wild type and Ryr1 mutant mice, revealing reduced RyR1 and altered protein content linked to congenital myopathies.
bioRxiv · Sep 26, 2022Physiology