Identification of RPGR ORF15 mutation for X-linked retinitis pigmentosa in a large Chinese family and in vitro correction with prime editor.
Gene Ther
; 30(1-2): 160-166, 2023 02.
Article
in En
| MEDLINE
| ID: mdl-35794468
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Retinitis Pigmentosa
/
Genetic Diseases, X-Linked
/
Eye Proteins
Type of study:
Diagnostic_studies
Limits:
Humans
Language:
En
Journal:
Gene Ther
Journal subject:
GENETICA MEDICA
/
TERAPEUTICA
Year:
2023
Type:
Article
Affiliation country:
China