TY  - GEN
AU  - Ali,Manir
AU  - Buentello-Volante,Beatriz
AU  - McKibbin,Martin
AU  - Rocha-Medina,J Alberto
AU  - Fernandez-Fuentes,Narcis
AU  - Koga-Nakamura,Wilson
AU  - Ashiq,Aruna
AU  - Khan,Kamron
AU  - Booth,Adam P
AU  - Williams,Grange
AU  - Raashid,Yasmin
AU  - Jafri,Hussain
AU  - Rice,Aine
AU  - Inglehearn,Chris F
AU  - Zenteno,Juan Carlos
TI  - Homozygous FOXE3 mutations cause non-syndromic, bilateral, total sclerocornea, aphakia, microphthalmia and optic disc coloboma
SN  - 1090-0535
PY  - 2010///1112
KW  - Amino Acid Sequence
KW  - Aphakia
KW  - complications
KW  - Base Sequence
KW  - Coloboma
KW  - Cornea
KW  - abnormalities
KW  - DNA Mutational Analysis
KW  - Family
KW  - Female
KW  - Forkhead Transcription Factors
KW  - chemistry
KW  - Homozygote
KW  - Humans
KW  - Male
KW  - Mexico
KW  - Microphthalmos
KW  - Molecular Sequence Data
KW  - Mutation
KW  - genetics
KW  - Optic Disk
KW  - Pakistan
KW  - Pedigree
KW  - Syndrome
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
ER  -