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; Gough, V; Rivera, RMC; Aartsma-Rus, A; Asokan, A; Gersbach, CA
Published in: MOLECULAR THERAPY
May 1, 2018
Duke Scholars
Published In
MOLECULAR THERAPY
EISSN
1525-0024
ISSN
1525-0016
Publication Date
May 1, 2018
Volume
26
Issue
5
Start / End Page
118 / 119
Location
Chicago, IL
Publisher
CELL PRESS
Conference Name
21st 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., Gough, V., Rivera, R. M. C., Aartsma-Rus, A., … Gersbach, C. A. (2018). Dystrophin Restoration in a Humanized Mouse Model of Duchenne Muscular Dystrophy by Gene Editing with S. Aureus Cas9. In MOLECULAR THERAPY (Vol. 26, pp. 118–119). Chicago, IL: CELL PRESS.
Robinson-Hamm, Jacqueline N., Christopher E. Nelson, Matthew Gemberling, Veronica Gough, 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, 26:118–19. CELL PRESS, 2018.
Robinson-Hamm JN, Nelson CE, Gemberling M, Gough V, Rivera RMC, Aartsma-Rus 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; 2018. p. 118–9.
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. 26, no. 5, CELL PRESS, 2018, pp. 118–19.
Robinson-Hamm JN, Nelson CE, Gemberling M, Gough V, 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; 2018. p. 118–119.
Published In
MOLECULAR THERAPY
EISSN
1525-0024
ISSN
1525-0016
Publication Date
May 1, 2018
Volume
26
Issue
5
Start / End Page
118 / 119
Location
Chicago, IL
Publisher
CELL PRESS
Conference Name
21st 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