Dystrophin Restoration in a Humanized Mouse Model of Duchenne Muscular Dystrophy by Gene Editing with S. aureus Cas9
Publication
, Conference
Robinson-Hamm, JN; Nelson, CE; Gemberling, M; Rivera, RMC; Aartsma-Rus, A; Asokan, A; Gersbach, CA
Published in: MOLECULAR THERAPY
May 1, 2017
Duke Scholars
Published In
MOLECULAR THERAPY
EISSN
1525-0024
ISSN
1525-0016
Publication Date
May 1, 2017
Volume
25
Issue
5
Start / End Page
17 / 17
Location
Washington, DC
Publisher
CELL PRESS
Conference Name
20th Annual Meeting of the American-Society-of-Gene-and-Cell-Therapy (ASGCT)
Related Subject Headings
- Biotechnology
- 3206 Medical biotechnology
- 3202 Clinical sciences
- 3105 Genetics
- 11 Medical and Health Sciences
- 10 Technology
- 06 Biological Sciences
Citation
APA
Chicago
ICMJE
MLA
NLM
Robinson-Hamm, J. N., Nelson, C. E., Gemberling, M., Rivera, R. M. C., Aartsma-Rus, A., Asokan, A., & Gersbach, C. A. (2017). Dystrophin Restoration in a Humanized Mouse Model of Duchenne Muscular Dystrophy by Gene Editing with S. aureus Cas9. In MOLECULAR THERAPY (Vol. 25, pp. 17–17). Washington, DC: CELL PRESS.
Robinson-Hamm, Jacqueline N., Christopher E. Nelson, Matthew Gemberling, Ruth M Castellanos Rivera, Annemieke Aartsma-Rus, Aravind Asokan, and Charles A. Gersbach. “Dystrophin Restoration in a Humanized Mouse Model of Duchenne Muscular Dystrophy by Gene Editing with S. aureus Cas9.” In MOLECULAR THERAPY, 25:17–17. CELL PRESS, 2017.
Robinson-Hamm JN, Nelson CE, Gemberling M, Rivera RMC, Aartsma-Rus A, Asokan A, et al. Dystrophin Restoration in a Humanized Mouse Model of Duchenne Muscular Dystrophy by Gene Editing with S. aureus Cas9. In: MOLECULAR THERAPY. CELL PRESS; 2017. p. 17–17.
Robinson-Hamm, Jacqueline N., et al. “Dystrophin Restoration in a Humanized Mouse Model of Duchenne Muscular Dystrophy by Gene Editing with S. aureus Cas9.” MOLECULAR THERAPY, vol. 25, no. 5, CELL PRESS, 2017, pp. 17–17.
Robinson-Hamm JN, Nelson CE, Gemberling M, Rivera RMC, Aartsma-Rus A, Asokan A, Gersbach CA. Dystrophin Restoration in a Humanized Mouse Model of Duchenne Muscular Dystrophy by Gene Editing with S. aureus Cas9. MOLECULAR THERAPY. CELL PRESS; 2017. p. 17–17.
Published In
MOLECULAR THERAPY
EISSN
1525-0024
ISSN
1525-0016
Publication Date
May 1, 2017
Volume
25
Issue
5
Start / End Page
17 / 17
Location
Washington, DC
Publisher
CELL PRESS
Conference Name
20th Annual Meeting of the American-Society-of-Gene-and-Cell-Therapy (ASGCT)
Related Subject Headings
- Biotechnology
- 3206 Medical biotechnology
- 3202 Clinical sciences
- 3105 Genetics
- 11 Medical and Health Sciences
- 10 Technology
- 06 Biological Sciences