Long-Term Therapeutic Efficacy of Intravenous AAV-Mediated Hamartin Replacement in Mouse Model of Tuberous Sclerosis Type 1.

Prabhakar S, Cheah PS, Zhang X, Zinter M, Gianatasio M, Hudry E, Bronson RT, Kwiatkowski DJ, Stemmer-Rachamimov A, Maguire CA, Sena-Esteves M, Tannous BA, Breakefield XO

Open source

DOI
10.1016/j.omtm.2019.08.003
Published
2019 Dec 13
Container
Molecular therapy. Methods & clinical development
Publisher
Not recorded
Open access
yes

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BibTeX

@article{allodium:10.1016/j.omtm.2019.08.003,
  title = {Long-Term Therapeutic Efficacy of Intravenous AAV-Mediated Hamartin Replacement in Mouse Model of Tuberous Sclerosis Type 1.},
  author = {Prabhakar S and Cheah PS and Zhang X and Zinter M and Gianatasio M and Hudry E and Bronson RT and Kwiatkowski DJ and Stemmer-Rachamimov A and Maguire CA and Sena-Esteves M and Tannous BA and Breakefield XO},
  year = {2019},
  journal = {Molecular therapy. Methods \& clinical development},
  doi = {10.1016/j.omtm.2019.08.003},
  url = {https://doi.org/10.1016/j.omtm.2019.08.003}
}

RIS

TY  - JOUR
TI  - Long-Term Therapeutic Efficacy of Intravenous AAV-Mediated Hamartin Replacement in Mouse Model of Tuberous Sclerosis Type 1.
AU  - Prabhakar S
AU  - Cheah PS
AU  - Zhang X
AU  - Zinter M
AU  - Gianatasio M
AU  - Hudry E
AU  - Bronson RT
AU  - Kwiatkowski DJ
AU  - Stemmer-Rachamimov A
AU  - Maguire CA
AU  - Sena-Esteves M
AU  - Tannous BA
AU  - Breakefield XO
PY  - 2019
JO  - Molecular therapy. Methods & clinical development
DO  - 10.1016/j.omtm.2019.08.003
UR  - https://doi.org/10.1016/j.omtm.2019.08.003
ER  - 

APA

S, P., PS, C., X, Z., M, Z., M, G., E, H., RT, B., DJ, K., A, S., CA, M., M, S., BA, T., & XO, B. (2019). Long-Term Therapeutic Efficacy of Intravenous AAV-Mediated Hamartin Replacement in Mouse Model of Tuberous Sclerosis Type 1.. Molecular therapy. Methods & clinical development. https://doi.org/10.1016/j.omtm.2019.08.003

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