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题目:: Modified patient stem cells as prelude to autologous treatment of muscular dystrophy.
作者:: Davies(Kay E),Grounds(Miranda D)
状态:: 发布时间2008-03-28 , 更新时间 2016-11-24
期刊:: Cell Stem Cell
摘要:: Duchenne muscular dystrophy is a devastating muscle wasting disease for which there is no effective treatment. In this issue of Cell Stem Cell, Benchaouir et al. (2007) demonstrate the delivery of genetically corrected CD133+ patient cells into mice, suggesting a new potential avenue for autologous cell therapy.
语言:: eng
DOI:: 10.1016/j.stem.2007.11.003

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