Single amino acid variation in MAB21L1 is dominantly associated with congenital eye defects.
J Med Genet
; 60(7): 655-661, 2023 07.
Article
in En
| MEDLINE
| ID: mdl-36446583
Key words
Full text:
1
Database:
MEDLINE
Main subject:
Eye Abnormalities
/
Microphthalmos
Type of study:
Prognostic_studies
/
Risk_factors_studies
Limits:
Humans
Language:
En
Year:
2023
Type:
Article