Siga,N.: "Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy." J.Clin.Invest.100.9. 2204-2210 (1997)
Siga,N.: "Disruption of the splicing enhancer sequence within exon 27 of the dystrophin gene by a nonsense mutation induces partial skipping of the exon and is responsible for Becker muscular dystrophy." J.Clin.Invest.100.9. 2204-2210 (1997)
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Siga,N.：“无义突变破坏肌营养不良蛋白基因外显子 27 内的剪接增强子序列会导致外显子部分跳跃，从而导致贝克尔肌营养不良症。”
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