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1دورية أكاديمية
المؤلفون: Chamberlain, Jeffrey S, Robb, Melissa, Braun, Serge, Brown, Kristy J, Danos, Olivier, Ganot, Annie, Gonzalez-Alegre, Pedro, Hunter, Nina, McDonald, Craig, Morris, Carl, Tobolowsky, Mark, Wagner, Kathryn R, Ziolkowski, Olivia, Duan, Dongsheng
المصدر: Human Gene Therapy. 34(9-10)
مصطلحات موضوعية: Medical Biotechnology, Biomedical and Clinical Sciences, Regenerative Medicine, Clinical Trials and Supportive Activities, Biotechnology, Intellectual and Developmental Disabilities (IDD), Gene Therapy, Orphan Drug, Duchenne/ Becker Muscular Dystrophy, Pediatric, Brain Disorders, Muscular Dystrophy, Rare Diseases, Genetics, Clinical Research, 5.2 Cellular and gene therapies, Development of treatments and therapeutic interventions, Musculoskeletal, Male, Humans, Muscular Dystrophy, Duchenne, Muscle, Skeletal, Genetic Therapy, Gene Transfer Techniques, Biomarkers, microdystrophin, Duchenne muscular dystrophy, gene therapy, AAV vector, Clinical Sciences, Medical biotechnology
وصف الملف: application/pdf
URL الوصول: https://escholarship.org/uc/item/0v56c0vk
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2دورية أكاديمية
المؤلفون: Boehler, Jessica F, Brown, Kristy J, Beatka, Margaret, Gonzalez, J Patrick, Donisa Dreghici, Roxana, Soustek-Kramer, Meghan, McGonigle, Sharon, Ganot, Annie, Palmer, Timothy, Lowie, Caitlin, Chamberlain, Jeffrey S., Lawlor, Michael W, Morris, Carl A
المصدر: In Neuromuscular Disorders January 2023 33(1):40-49
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3دورية
المؤلفون: Cope, Heidi, Fischer, Ryan, Heslop, Emma, McNiff, Megan, Johnson, Alexandra, Camino, Eric, Denger, Brian, Armstrong, Niki, Thakrar, Sejal, Bateman-House, Alison, Beaverson, Katherine L., Woollacott, Ione O.C., Phillips, Dawn, Fernandez, Vivian, Ganot, Annie, Donisa-Dreghici, Roxana, Mansfield, Carol, Peay, Holly
المصدر: Journal of Neuromuscular Diseases; 20240101, Issue: Preprints p1-9, 9p
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4دورية أكاديمية
المؤلفون: Paquin, Ryan S.Aff1, Fischer, RyanAff2, Mansfield, CarolAff3, Mange, BrennanAff3, Beaverson, KatherineAff4, Ganot, AnnieAff5, Martin, Amy StrongAff6, Morris, CarlAff5, Rensch, ColinAff2, Ricotti, ValeriaAff5, Russo, Leo J.Aff4, Sadosky, AlesiaAff4, Smith, Edward C.Aff7, Peay, Holly L.Aff1
المصدر: Orphanet Journal of Rare Diseases. 14(1)
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5دورية أكاديمية
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