Haghighi, Alireza <br/><br/>
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 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1090-0535 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Base Sequence<br/>Blepharophimosis--genetics<br/>DNA Mutational Analysis<br/>Female<br/>Forkhead Box Protein L2<br/>Forkhead Transcription Factors--genetics<br/>Genes, Dominant<br/>Genetic Linkage<br/>Genotype<br/>Heterozygote<br/>Humans<br/>Iran<br/>Male<br/>Molecular Sequence Data<br/>Mutation, Missense<br/>Pedigree<br/>Phenotype<br/>Protein Structure, Tertiary<br/>Severity of Illness Index<br/>Skin Abnormalities--genetics