Identification and Functional Characterization of Mutation in FYCO1 in Families with Congenital Cataract.
Life (Basel)
; 13(8)2023 Aug 21.
Article
in En
| MEDLINE
| ID: mdl-37629644
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Type of study:
Diagnostic_studies
Language:
En
Journal:
Life (Basel)
Year:
2023
Document type:
Article
Affiliation country:
Country of publication: