CRISPR-Cas9 In Vivo Gene Editing for Transthyretin Amyloidosis

Julian D. Gillmore(Alnylam Pharmaceuticals (United States)), David Lebwohl(Intellia Therapeutics (United States)), Andrew Schiermeier(University of Auckland), Jonathan A. Phillips(Boehringer Ingelheim (United States)), David E. Gutstein(Scripps Research Institute), Olivier Harari(Regeneron (United States)), Kristy Wood(University of Auckland), Michael L. Maitland(Virginia Cancer Institute), Randy Soltys(University of Auckland), Brian Zambrowicz(Regeneron (United States)), Laura Sepp‐Lorenzino(Intellia Therapeutics (United States)), Yuanxin Xu(Nanjing University of Chinese Medicine), Marianna Fontana(Amyloidosis Foundation), Adam Amaral(University of Auckland), Christos A. Kyratsous(Regeneron (United States)), Daniel J. O’Connell(Harvard University), Jörg Täubel(British Heart Foundation), Kathryn Walsh(University of Auckland), Mark D. McKee(University of Auckland), Adam P. Boyd(University of Auckland), Justin Kao(University of Auckland), Ed Gane(University of Auckland), John P. Leonard(Institute of Genetics), Andrew Murphy(University of Auckland), Jeffrey Cehelsky(Alnylam Pharmaceuticals (United States)), Jessica Seitzer(Intellia Therapeutics (United States))
New England Journal of Medicine
June 26, 2021
Cited by 1,694


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