Natural Disease Course in Usher Syndrome Patients Harboring
USH2A
Usher syndrome
exon skipping therapy
fundus autofluorescence
retinitis pigmentosa
Journal
Genes
ISSN: 2073-4425
Titre abrégé: Genes (Basel)
Pays: Switzerland
ID NLM: 101551097
Informations de publication
Date de publication:
05 03 2023
05 03 2023
Historique:
received:
08
12
2022
revised:
08
02
2023
accepted:
13
02
2023
medline:
30
3
2023
entrez:
29
3
2023
pubmed:
30
3
2023
Statut:
epublish
Résumé
The aim of the study was to determine the rate of retinal degeneration in patients with c.2610C>A (p.Cys870*) in
Identifiants
pubmed: 36980924
pii: genes14030652
doi: 10.3390/genes14030652
pmc: PMC10048357
pii:
doi:
Substances chimiques
USH2A protein, human
0
Extracellular Matrix Proteins
0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
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