Towards a one‐time cure for Fabry disease: Lentivirus‐mediated haematopoietic stem and progenitor cell gene therapy

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Publication Details

Journal
Clinical and Translational Discovery
Published
2025-03-11
DOI
https://doi.org/10.1002/ctd2.70042
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
0.00
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article

Towards a one‐time cure for Fabry disease: Lentivirus‐mediated haematopoietic stem and progenitor cell gene therapy

Rina Kansal
Clinical and Translational Discovery
Lysosomal Storage Disorders Research
article

Towards a one‐time cure for Fabry disease: Lentivirus‐mediated haematopoietic stem and progenitor cell gene therapy

Rina Kansal
article en

Abstract

No abstract available for this paper.
Clinical and Translational DiscoveryVol. 5(2)
Versiti Blood Center of Wisconsin (US), University at Buffalo, State University of New York (US)
Zero hunger
Openalex Percentile: Top 94%
Lysosomal Storage Disorders Research
DOIOpen Access PDFOpenAlex
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Towards a one‐time cure for Fabry disease: Lentivirus‐mediated haematopoietic stem and progenitor cell gene therapy — Rina Kansal · Clinical and Translational Discovery (2025) | TGRS Research Map | TGRS