ABCA4 c.859-25A>G, a Frequent Palestinian Founder Mutation Affecting the Intron 7 Branchpoint, Is Associated With Early-Onset Stargardt Disease.
Invest Ophthalmol Vis Sci
; 63(4): 20, 2022 04 01.
Article
in En
| MEDLINE
| ID: mdl-35475888
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Introns
/
Arabs
/
Cone-Rod Dystrophies
/
Stargardt Disease
Type of study:
Risk_factors_studies
Limits:
Humans
Language:
En
Journal:
Invest Ophthalmol Vis Sci
Year:
2022
Document type:
Article
Affiliation country: