The Clinical, Myopathological, and Genetic Analysis of 20 Patients With Non-dystrophic Myotonia
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DOI: 10.3389/fneur.2022.830707
Abstract: Introduction Non-dystrophic myotonias (NDMs) are skeletal muscle ion channelopathies caused by CLCN1 or SCN4A mutations. This study aimed to describe the clinical, myopathological, and genetic analysis of NDM in a large Chinese cohort. Methods We… read more here.
Keywords: myotonia; pmc patients; muscle; pathology ... See more keywords