Phenotypic overlap between familial exudative vitreoretinopathy and microcephaly, lymphedema, and chorioretinal dysplasia caused by KIF11 mutations.
JAMA Ophthalmol
; 132(12): 1393-9, 2014 Dec.
Article
in En
| MEDLINE
| ID: mdl-25124931
Full text:
1
Collection:
01-internacional
Database:
MEDLINE
Main subject:
Retinal Dysplasia
/
Kinesins
/
Lymphedema
/
Microcephaly
/
Mutation
Type of study:
Diagnostic_studies
/
Prognostic_studies
Limits:
Child
/
Child, preschool
/
Female
/
Humans
/
Male
Language:
En
Journal:
JAMA Ophthalmol
Year:
2014
Document type:
Article
Affiliation country:
Canada
Country of publication:
United States