Family-based exome sequencing identifies rare coding variants in age-related macular degeneration.
Hum Mol Genet
; 29(12): 2022-2034, 2020 07 29.
Article
in En
| MEDLINE
| ID: mdl-32246154
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Genetic Predisposition to Disease
/
Receptors, KIR2DL4
/
Genome-Wide Association Study
/
NAV1.8 Voltage-Gated Sodium Channel
/
Macular Degeneration
Limits:
Aged
/
Aged80
/
Humans
/
Male
/
Middle aged
Language:
En
Journal:
Hum Mol Genet
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2020
Document type:
Article
Affiliation country:
United States
Country of publication:
United kingdom