Identification of novel homozygous variants in FOXE3 and AP4M1 underlying congenital syndromic anophthalmia and microphthalmia.
J Gene Med
; 26(1): e3601, 2024 Jan.
Article
in En
| MEDLINE
| ID: mdl-37758467
Key words
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Anophthalmos
/
Microphthalmos
Type of study:
Diagnostic_studies
/
Guideline
/
Prognostic_studies
Limits:
Humans
Language:
En
Journal:
J Gene Med
Journal subject:
BIOLOGIA MOLECULAR
/
GENETICA MEDICA
Year:
2024
Type:
Article
Affiliation country:
Pakistan