Change in Cone Structure Over 24 Months in USH2A-Related Retinal Degeneration

Author:

Duncan Jacque L.ORCID,Liang Wendi,Maguire Maureen G.,Porco Travis C.,Wong Jessica,Audo Isabelle,Cava Jenna A.,Grieve Kate,Kalitzeos Angelos,Kreis Joseph,Michaelides Michel,Norberg Nathaniel,Paques Michel,Carroll Joseph

Publisher

Elsevier BV

Subject

Ophthalmology

Reference55 articles.

1. Daiger SP. Summaries of genes and loci causing retinal diseases. Available at https://web.sph.uth.edu/RetNet/sum-dis.htm. Accessed December 22, 2022.

2. Tissue-specific genotype-phenotype correlations among USH2A-related disorders in the RUSH2A study;Hufnagel;Hum Mutat,2022

3. Expanding the clinical and molecular heterogeneity of nonsyndromic inherited retinal dystrophies;Rodríguez-Muñoz;J Mol Diagn,2020

4. Phenotypic variability of recessive RDH12-associated retinal dystrophy;Zou;Retina,2019

5. Clinical evidence for the importance of the wild-type PRPF31 allele in the phenotypic expression of RP11;Roshandel;Genes (Basel),2021

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