Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma. [electronic resource]
Producer: 20101112Description: 1162-8 p. digitalISSN:- 1090-0535
- Amino Acid Sequence
- Aphakia -- complications
- Base Sequence
- Coloboma -- complications
- Cornea -- abnormalities
- DNA Mutational Analysis
- Family
- Female
- Forkhead Transcription Factors -- chemistry
- Homozygote
- Humans
- Male
- Mexico
- Microphthalmos -- complications
- Molecular Sequence Data
- Mutation -- genetics
- Optic Disk -- abnormalities
- Pakistan
- Pedigree
- Syndrome
No physical items for this record
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.