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X连锁肌萎缩的遗传服务Dystrophin基因的缺失突变可引起病情严重的DMD或病情较轻的BMD,有两个高频缺失区(HFDR)分别位于dystrophin基因5′端下游500及1200kb处。我们改进
Genetics Services for X-Chain Muscle Depression A deletion mutation in the Dystrophin gene can cause a serious DMD or less severe BMD with two high-frequency deletion (HFDR) sites 500 and 1200 kb downstream of the 5 ’end of the dystrophin gene, respectively. We improve