Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration-Reference-Cited by-同舟云学术

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Investigating G-quadruplex structures in RPGR gene: Implications for understanding X-linked retinal degeneration

Published:2024-04 Issue:8 Volume:10 Page:e29828
ISSN:2405-8440
Container-title:Heliyon
language:en
Short-container-title:Heliyon

Author:

Donato Luigi^ORCID,Scimone Concetta,Alibrandi Simona,Mordà Domenico,Anchesi Ivan,Scalinci Sergio Zaccaria,Rinaldi Carmela,D'Angelo Rosalia,Sidoti Antonina

Publisher

Elsevier BV

Reference45 articles.

1. Inherited retinal diseases: linking genes, disease-causing variants, and relevant therapeutic modalities;Schneider;Prog. Retin. Eye Res.,2022

2. The impact of modifier genes on cone-rod dystrophy heterogeneity: an explorative familial pilot study and a hypothesis on neurotransmission impairment;Donato;PLoS One,2022

3. Epitranscriptome analysis of oxidative stressed retinal epithelial cells depicted a possible RNA editing landscape of retinal degeneration;Donato;Antioxidants,2022

4. Genetic landscape of 6089 inherited retinal dystrophies affected cases in Spain and their therapeutic and extended epidemiological implications;Perea-Romero;Sci. Rep.,2021

5. Genetic testing and diagnosis of inherited retinal diseases;Lam;Orphanet J. Rare Dis.,2021

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