TY  - GEN
AU  - Haghighi,Alireza
AU  - Verdin,Hannah
AU  - Haghighi-Kakhki,Hamidreza
AU  - Piri,Niloofar
AU  - Gohari,Nasrollah Saleh
AU  - De Baere,Elfride
TI  - Missense mutation outside the forkhead domain of FOXL2 causes a severe form of BPES type II
SN  - 1090-0535
PY  - 2012///0717
KW  - Base Sequence
KW  - Blepharophimosis
KW  - genetics
KW  - DNA Mutational Analysis
KW  - Female
KW  - Forkhead Box Protein L2
KW  - Forkhead Transcription Factors
KW  - Genes, Dominant
KW  - Genetic Linkage
KW  - Genotype
KW  - Heterozygote
KW  - Humans
KW  - Iran
KW  - Male
KW  - Molecular Sequence Data
KW  - Mutation, Missense
KW  - Pedigree
KW  - Phenotype
KW  - Protein Structure, Tertiary
KW  - Severity of Illness Index
KW  - Skin Abnormalities
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
ER  -