Lack of FOXE3 coding mutation in a case of congenital aphakia.

Sano, Yusuke

Lack of FOXE3 coding mutation in a case of congenital aphakia. [electronic resource] - Ophthalmic genetics - 95-98 p. digital

Publication Type: Case Reports; Journal Article

1744-5094

10.1080/13816810.2017.1350722 doi


Anterior Eye Segment--abnormalities
Aphakia--congenital
Axial Length, Eye--pathology
Child, Preschool
DNA Mutational Analysis
Forkhead Transcription Factors--genetics
Humans
Magnetic Resonance Imaging
Male
Microphthalmos--genetics
Microscopy, Acoustic
Mutation
Polymerase Chain Reaction
Exome Sequencing