Persistent hematopoietic polyclonality after lentivirus-mediated gene therapy for Fabry disease
Author:
Funder
Canadian Institutes of Health Research
Kidney Foundation of Canada
MACC Fund
Publisher
Elsevier BV
Subject
Genetics,Molecular Biology,Molecular Medicine
Reference26 articles.
1. Fabry's disease;Zarate;Lancet,2008
2. Fabry disease revisited: management and treatment recommendations for adult patients;Ortiz;Mol. Genet. Metab.,2018
3. Lentivirus-mediated gene therapy for Fabry disease;Khan;Nat. Commun.,2021
4. LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1;Hacein-Bey-Abina;Science,2003
5. Insertional oncogenesis in 4 patients after retrovirus-mediated gene therapy of SCID-X1;Hacein-Bey-Abina;J. Clin. Invest.,2008
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3. A mass spectrometry assay for detection of endogenous and lentiviral engineered hemoglobin in cultured cells and sickle cell disease mice;The Journal of Gene Medicine;2023-07-17
4. Fabry disease: current treatment and future perspective;Journal of Genetic Medicine;2023-06-30
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