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Myofibrillar Myopathy 11
A myofibrillar myopathy that is characterized by onset of slowly progressive proximal muscle weakness in the first decade of life and that is caused by homozygous or compound heterozygous mutation in the UNC45B gene on c
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Overview
A myofibrillar myopathy that is characterized by onset of slowly progressive proximal muscle weakness in the first decade of life and that is caused by homozygous or compound heterozygous mutation in the UNC45B gene on c
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