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Meet the family working with scientists to fight rare diseases with CRISPR therapy

shannon.ashoori Message
23 Jun 2020, 10:32 PM

Check out this story about Terry Horgan, a 24 year old boy, living with muscular dystrophy. Terry’s brother has founded “Cure Rare Disease”, a non profit organization which is currently exploring a treatment for muscular dystrophy. This new gene editing technique is called CRISPR. Watch the video within the provided link to learn more!

https://www.today.com/video/meet-the-family-working-with-scientists-to-fight-rare-diseases-with-crispr-therapy-85361221934

shannon.ashoori Message
23 Jun 2020, 10:32 PM