Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II.

Haghighi, Alireza

Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II. [electronic resource] - Molecular vision 2012 - 211-8 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1090-0535


Base Sequence
Blepharophimosis--genetics
DNA Mutational Analysis
Female
Forkhead Box Protein L2
Forkhead Transcription Factors--genetics
Genes, Dominant
Genetic Linkage
Genotype
Heterozygote
Humans
Iran
Male
Molecular Sequence Data
Mutation, Missense
Pedigree
Phenotype
Protein Structure, Tertiary
Severity of Illness Index
Skin Abnormalities--genetics