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A Novel Mutation in N-Terminal Actin-Binding Domain of the DMD Gene Presenting Becker Muscular Dystrophy as Recurrent Exertional Rhabdomyolysis: A Case Report.
Annals of Indian Academy of Neurology ( IF 1.7 ) Pub Date : 2020 , DOI: 10.4103/aian.aian_215_19 Jong-Mok Lee 1
中文翻译:
一种新型突变的DMD基因的N末端肌动蛋白结合域呈现贝克肌营养不良症为反复性横纹肌溶解:病例报告。
更新日期:2020-02-05
Annals of Indian Academy of Neurology ( IF 1.7 ) Pub Date : 2020 , DOI: 10.4103/aian.aian_215_19 Jong-Mok Lee 1
Affiliation
中文翻译:
一种新型突变的DMD基因的N末端肌动蛋白结合域呈现贝克肌营养不良症为反复性横纹肌溶解:病例报告。