Facioscapulohumeral Muscular Dystrophy Type 2 due to a Novel Pathogenic Variant (c.180_183delGTGT: p.Cys61ArgfsX47) in the SMCHD1 Gene, Confirmed by Molecular Testing: A Case Report

被引:0
作者
Cuchanski, Mathieu [1 ]
Morren, John [2 ]
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[1] Cleveland Clin, Neuromuscular Ctr, Cleveland, OH 44106 USA
[2] Cleveland Clin, Cleveland, OH USA
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R74 [神经病学与精神病学];
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4628
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页数:2
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