Published in
American Association for the Advancement of Science, Science Translational Medicine, 536(12), 2020
DOI: 10.1126/scitranslmed.aay0271
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Applying genome-wide CRISPR-Cas9 screens for therapeutic discovery in facioscapulohumeral muscular dystrophy
Journal article published in 2020 by
Angela Lek 
,
Yuanfan Zhang ,
Keryn G. Woodman ,
Shushu Huang,
Alec M. DeSimone ,
Justin Cohen ,
Vincent Ho,
James Conner ,
Lillian Mead ,
Andrew Kodani ,
Anna Pakula,
Neville Sanjana ,
Oliver D. King,
Peter L. Jones,
Kathryn R. Wagner
and other authors.
,
Yuanfan Zhang ,
Keryn G. Woodman ,
Shushu Huang,
Alec M. DeSimone ,
Justin Cohen ,
Vincent Ho,
James Conner ,
Lillian Mead ,
Andrew Kodani ,
Anna Pakula,
Neville Sanjana ,
Oliver D. King,
Peter L. Jones,
Kathryn R. Wagner
and other authors.
This paper was not found in any repository, but could be made available legally by the author.
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Abstract
Genome-wide CRISPR-Cas9 screens identify druggable pathways associated with facioscapulohumeral muscular dystrophy.