在肌营养不良蛋白基因，在人类基因大多数，这种遗传信息不连续的。
In the dystrophin gene, and in most of human genes, this genetic information is not contiguous.
DMD是九种肌营养不良症的最常见类型，以缺少四肢等随意肌的肌营养不良蛋白为主要特征。
DMD is the most common of nine types of muscular dystrophy, which is characterized by a lack of the protein dystrophin in voluntary muscles, such as those in the arms and legs.
并采用免疫荧光抗体染色技术对5例dmd, 2例BMD肌细胞膜上抗肌营养不良蛋白的表达观察分析，以2例正常人的肌组织作为对照。
The patients from 5 DMD and 2 BMD were detected by immunofluorescence technique for analyzing dystrophin located in muscle cell membrane, compared with 2 normal males.
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