In the dystrophin gene, and in most of human genes, this genetic information is not contiguous.
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。
The dystrophin gene is found on the X chromosome and passed on to children through a mother who is a carrier.
肌营养不良卵白基因位于人类X染色体，携带基因突变的母亲会遗传给婴儿。
It is important to note, however, that different mutations in the dystrophin gene could require different oligonucleotide drugs.
重要的是要注意，不过，在不同的肌营养不良基因突变可能需要不同的寡核苷酸药物。
Wu et al, Effective rescue of dystrophin improves cardiac function in dystrophin-deficient mice by a modified morpholino oligomer.
吴等人，有效的抗肌萎缩蛋白拯救提高了修改吗啉齐聚心功能的抗肌萎缩缺陷小鼠。
This new research modified the introduced dystrophin gene to increase the efficiency of dystrophin protein production in the cells.
这一新的经过改造的方法，增强了抗肌萎缩蛋白在肌肉细胞内产生的有效性。
In these trials, dystrophin-positive fibres were accounted for by transcriptional (revertant) variants of the mutant dystrophin transcript.
在这些试验中，营养不良素阳性的肌纤维是由营养不良素转录体的突变引起的。
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.
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。
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.
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.
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。
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