A novel variant in FOXC1 associated with atypical Axenfeld-Rieger syndrome.
BMC Med Genomics
; 14(1): 277, 2021 11 22.
Article
in En
| MEDLINE
| ID: mdl-34809627
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Eye Diseases, Hereditary
/
Eye Abnormalities
Type of study:
Diagnostic_studies
/
Guideline
/
Prognostic_studies
/
Risk_factors_studies
Limits:
Child, preschool
/
Humans
/
Male
Language:
En
Journal:
BMC Med Genomics
Journal subject:
GENETICA MEDICA
Year:
2021
Type:
Article