Gene therapy in children with AIPL1-associated severe retinal dystrophy: an open-label, first-in-human interventional study

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Publication Details

Journal
The Lancet
Published
2025-02-01
DOI
https://doi.org/10.1016/s0140-6736(24)02812-5
Citations
13
Primary Topic
Retinal Development and Disorders
Type
article
Field-Weighted Citation Impact
10.48

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article

Gene therapy in children with AIPL1-associated severe retinal dystrophy: an open-label, first-in-human interventional study

Neruban Kumaran, Angelos Kalitzeos, Anastasios Georgiadis, Jacqueline van der Spuy et al.
13 citations
The Lancet
Retinal Development and Disorders
10.48
article

Gene therapy in children with AIPL1-associated severe retinal dystrophy: an open-label, first-in-human interventional study

Neruban Kumaran, Angelos Kalitzeos, Anastasios Georgiadis, Jacqueline van der Spuy, Serena Zaman, Alexandria Forbes, Vijay Tailor, Sui Chien Wong, Ngozi Oluonye, Yannik Laich, Roni O. Maimon-Mor, James Bainbridge, Pete R. Jones, Harry Petrushkin, Eugene R Arulmuthu, Robin R. Ali, Marc Pabst, Michel Michaelides, Tessa M. Dekker, Alexander J. Smith, Stuart Naylor, Michalis Georgiou, Kim Staeubli, Steven H Scholte
article en
13 citations

Abstract

No abstract available for this paper.
The LancetVol. 405(10479)
University College London (GB), University of Amsterdam (NL)
National Institute for Health and Care Research, Santen, Moorfields Eye Charity, Medical Research Council, National Institute for Health Research Biomedical Research Centre at Moorfields Eye Hospital NHS Foundation Trust and UCL Institute of Ophthalmology
Openalex Percentile: Top 1%
Retinal Development and Disorders
10.48
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