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publicationName Molecular therapy : the journal of the American Society of Gene Therapy
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bibliographicCitation Wang Y, Hao L, Wang H, Santostefano K, Thapa A, Cleary J, Li H, Guo X, Terada N, Ashizawa T, Xia G. Therapeutic Genome Editing for Myotonic Dystrophy Type 1 Using CRISPR/Cas9. Molecular Therapy. 2018 Nov;26(11):2617–30. doi: 10.1016/j.ymthe.2018.09.003.
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title Therapeutic Genome Editing for Myotonic Dystrophy Type 1 Using CRISPR/Cas9
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