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Centronuclear myopathy (CNM) is characterized by a pathological finding of central nuclei. Sporadic or autosomal dominant CNM is linked to a gene encoding dynamin 2 (DNM2) while autosomal recessive and X-linked form are related to BIN1 and MTM1, respectively. Clinical spectrum of CNM is ranged from severe to mild phenotypes. We are to analyze clinical and pathological features of sporadic CNM patients...
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