Lack of FOXE3 coding mutation in a case of congenital aphakia. [electronic resource]
Producer: 20180326Description: 95-98 p. digitalISSN:- 1744-5094
- 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
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Publication Type: Case Reports; Journal Article
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