Myopathies are a clinically and genetically heterogenous group of
muscle diseases characterized by pathologic changes in muscle
fibres that compromise their contractile ability. The authors of
this book have gathered new research from across the globe and
topics discussed in this compilation include inherited myopathies
with distinct clinical manifestations; muscle biopsy as a
diagnostic procedure in suspected myopathies; inflammation in
dysferlinopathies; mitochondrial disorders; dysphagia in the
myopathies; and aB-Crystallin (HSPB5) and myofibrillar myopathies.
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