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CRISPR-based gene editing shows promise in treating rare form of blindness

About 79% of clinical trial participants experienced measurable improvement after receiving experimental, CRISPR-based gene editing that is designed to fix a rare form of blindness, according to a paper published in the New England Journal of Medicine.

United statesAnn arborUniversity of pennsylvaniaBaisong meiMark pennesiTomass alemanScheie eye instituteBascom palmer eye institute in miamiUniversity of pennsylvania scheie eye instituteOregon health science universityKellogg eye centerCasey eye instituteNew england journalOregon healthScience universityLeber congenital amaurosis

OHSU Gene Editing Study Success | News Radio 1190 KEX

OHSU Gene Editing Study Success | News Radio 1190 KEX
iheart.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from iheart.com Daily Mail and Mail on Sunday newspapers.

United statesAnn arborUniversity of pennsylvaniaMark pennesiBaisong meiTomass alemanBascom palmer eye institute in miamiUniversity of pennsylvania scheie eye instituteKellogg eye centerScheie eye instituteOregon health science universityCasey eye instituteNew england journalOregon healthScience universityEditas medicine

CRISPR Gene Editing Shows Promise: Early Trial Improves Vision in Blind Children

Gene therapy has shown promise in improving eyesight in congenitally blind children with Leber Congenital Amaurosis (LCA), a rare disease.

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Editas Medicine (EDIT) Set to Announce Quarterly Earnings on Wednesday

Editas Medicine (EDIT) Set to Announce Quarterly Earnings on Wednesday
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Gene Therapy Improves Vision in People With Inherited Blindness

Key Takeaways

United statesUnited kingdomTomas alemanMark pennesiBaisong meiBascom palmer eye institute in miamiWk kellogg eye centerEar ocular genomics instituteScheie eye instituteOregon health science universityHealthday newsLeber congenital amaurosisNew england journalEric pierceMass eyeBerman gund laboratory