Mutation spectrum and genotype-phenotype correlations in Chinese congenital ectopia lentis patients.
Exp Eye Res
; 207: 108570, 2021 06.
Article
in En
| MEDLINE
| ID: mdl-33844962
Full text:
1
Database:
MEDLINE
Main subject:
Ectopia Lentis
/
Mutation, Missense
/
Asian People
/
Fibrillin-1
Type of study:
Observational_studies
/
Risk_factors_studies
Limits:
Adolescent
/
Adult
/
Child
/
Child, preschool
/
Female
/
Humans
/
Male
/
Middle aged
Country/Region as subject:
Asia
Language:
En
Year:
2021
Type:
Article