Sub-cellular level resolution of common genetic variation in the photoreceptor layer identifies continuum between rare disease and common variation.
PLoS Genet
; 19(2): e1010587, 2023 02.
Article
in En
| MEDLINE
| ID: mdl-36848389
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Rare Diseases
/
Genome-Wide Association Study
Limits:
Humans
Language:
En
Journal:
PLoS Genet
Journal subject:
GENETICA
Year:
2023
Document type:
Article
Affiliation country:
Reino Unido