Biochemical and pathological changes result from mutated Caveolin-3 in muscle

被引:0
作者
José Andrés González Coraspe
Joachim Weis
Mary E. Anderson
Ute Münchberg
Kristina Lorenz
Stephan Buchkremer
Stephanie Carr
René Peiman Zahedi
Eva Brauers
Hannah Michels
Yoshihide Sunada
Hanns Lochmüller
Kevin P. Campbell
Erik Freier
Denisa Hathazi
Andreas Roos
机构
[1] RWTH Aachen University Hospital,Institute of Neuropathology
[2] University of Iowa,Howard Hughes Medical Institute, Departments of Molecular Physiology and Biophysics, of Neurology
[3] Leibniz-Institut für Analytische Wissenschaften - ISAS - e.V,Biomedical Research Department, Tissue Omics group
[4] Institute of Genetic Medicine,Gerald Bronfman Department of Oncology
[5] International Centre for Life,Segal Cancer Proteomics Centre, Lady Davis Institute
[6] Jewish General Hospital,Department of Neurology
[7] McGill University,Department of Neuropediatrics and Muscle Disorders
[8] Jewish General Hospital,Centro Nacional de Análisis Genómico (CNAG
[9] McGill University,CRG)
[10] Kawasaki Medical School,Children’s Hospital of Eastern Ontario Research Institute
[11] Medical Center – University of Freiburg,undefined
[12] Faculty of Medicine,undefined
[13] Center for Genomic Regulation,undefined
[14] Barcelona Institute of Science and Technology (BIST),undefined
[15] University of Ottawa,undefined
[16] Ottawa,undefined
[17] Canada and Division of Neurology,undefined
[18] Department of Medicine,undefined
[19] The Ottawa Hospital,undefined
来源
Skeletal Muscle | / 8卷
关键词
Caveolin-3; Caveolinopathy; LGMD1C; Chaperonopathy; Protein aggregate; Skeletal muscle proteomics;
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