Development of CRISPR_SCD001, an Autologous Hematopoietic Stem Cell Gene Therapy for Sickle Cell Disease after CRISPR-Cas9 Mediated Correction.

DeWitt M, Campo-Fernandez B, Roy S, Kleinhenz ALW, Davila A, Lennon M, Vu JT, Krishnappa N, Said S, Tseng CH, Park SH, Bao G, Magis W, Martin DIK, Boffelli D, Wyman SK, Kohn DB, Walters MC, Romero Z

Open source

DOI
10.1016/j.ymthe.2026.09.020
Published
2026 Sep 19
Container
Molecular therapy : the journal of the American Society of Gene Therapy
Publisher
Not recorded
Open access
unknown

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BibTeX

@article{allodium:10.1016/j.ymthe.2026.09.020,
  title = {Development of CRISPR\_SCD001, an Autologous Hematopoietic Stem Cell Gene Therapy for Sickle Cell Disease after CRISPR-Cas9 Mediated Correction.},
  author = {DeWitt M and Campo-Fernandez B and Roy S and Kleinhenz ALW and Davila A and Lennon M and Vu JT and Krishnappa N and Said S and Tseng CH and Park SH and Bao G and Magis W and Martin DIK and Boffelli D and Wyman SK and Kohn DB and Walters MC and Romero Z},
  year = {2026},
  journal = {Molecular therapy : the journal of the American Society of Gene Therapy},
  doi = {10.1016/j.ymthe.2026.09.020},
  url = {https://doi.org/10.1016/j.ymthe.2026.09.020}
}

RIS

TY  - JOUR
TI  - Development of CRISPR_SCD001, an Autologous Hematopoietic Stem Cell Gene Therapy for Sickle Cell Disease after CRISPR-Cas9 Mediated Correction.
AU  - DeWitt M
AU  - Campo-Fernandez B
AU  - Roy S
AU  - Kleinhenz ALW
AU  - Davila A
AU  - Lennon M
AU  - Vu JT
AU  - Krishnappa N
AU  - Said S
AU  - Tseng CH
AU  - Park SH
AU  - Bao G
AU  - Magis W
AU  - Martin DIK
AU  - Boffelli D
AU  - Wyman SK
AU  - Kohn DB
AU  - Walters MC
AU  - Romero Z
PY  - 2026
JO  - Molecular therapy : the journal of the American Society of Gene Therapy
DO  - 10.1016/j.ymthe.2026.09.020
UR  - https://doi.org/10.1016/j.ymthe.2026.09.020
ER  - 

APA

M, D., B, C., S, R., ALW, K., A, D., M, L., JT, V., N, K., S, S., CH, T., SH, P., G, B., W, M., DIK, M., D, B., SK, W., DB, K., MC, W., & Z, R. (2026). Development of CRISPR_SCD001, an Autologous Hematopoietic Stem Cell Gene Therapy for Sickle Cell Disease after CRISPR-Cas9 Mediated Correction.. Molecular therapy : the journal of the American Society of Gene Therapy. https://doi.org/10.1016/j.ymthe.2026.09.020

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