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Events | 2016.01.16

Gene editing shows promise in treating muscular dystrophy - Ars Technica


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Gene editing shows promise in treating muscular dystrophy
Ars Technica
These experiments show exciting promise for the use of CRISPR in mammalian gene editing , which could eventually lead to cures for this and other genetic diseases in humans. Muscular dystrophy is a group of diseases that result in muscle weakness in ...
Researchers bring gene editing to patients with deadly diseases Medical Xpress
Genome editing treats muscular dystrophy in mice BioNews
2 teams of scientists are fighting over a powerful gene editing technology ... Yahoo Finance UK
EIN News (press release)  - Nature.com
all 17 news articles »

 

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