Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
June 28, 2024American Journal of OphthalmologyOpen Access

RDH5 and RLBP1-Associated Inherited Retinal Diseases: Refining the Spectrum of Stationary and Progressive Phenotypes

View Full Paper
Ask AI
Bookmark
Share

Authors

LBLorenzo BiancoAAAlessio AntropoliABAmine Benadji

Discussion

Loading...

Member takes

Overview

Key Points

Key points are not available for this paper at this time.

Cite This Study

Bianco et al. (2024) studied this question.

synapsesocial.com/papers/68e62ad5b6db6435875bdf57https://doi.org/10.1016/j.ajo.2024.06.016
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Biallelic RDH11 variants cause syndromic retinitis pigmentosa with early-onset cataracts and neurodevelopmental delay: a multicenter case series2026
  2. 2<i>RHO</i>-Associated Retinitis Pigmentosa: Genetics, Phenotype, Natural History, Functional Assays, and Animal Model – In Preparation for Clinical Trials2025 · 11 citations
  3. 3Dual CRALBP isoforms unveiled: iPSC-derived retinal modelling and AAV2/5-RLBP1 gene transfer raise considerations for effective therapy2024
  4. 4Functional and Structural Characterization of a Large Animal Model of <i>RDH5</i> -Associated Retinopathy2026
  5. 5Frequency and Genetic Spectrum of Inherited Retinal Dystrophies in a Large Dutch Pediatric Cohort: The RD5000 Consortium2024 · 2 citations