Gene Editing in Live Mice Cures Rare Liver Disease

Scientists at MIT have successfully used the CRISPR method to replace faulty genes in live mice, curing a rare liver disease. This type of genetic modification has been done in the past, but only in vitro [think petri dish]. Making this a monumental step forward for curing people who are suffering from genetic disease.

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April 3, 2014 | Categories: Genetics | Tags: CRISPR, DNA, future, Genetics, health, medicine, science | 2 Comments