Seifi, Morteza <br/><br/>
Novel PITX2 gene mutations in patients with Axenfeld-Rieger syndrome.  [electronic resource] 

 -  Acta ophthalmologica  Nov 2016 
 - e571-e579 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article 
<br/><br/><label>ISSN: </label>1755-3768 
<br/><br/><label>Standard No.: </label>10.1111/aos.13030  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Anterior Eye Segment--abnormalities<br/>Child, Preschool<br/>Consanguinity<br/>DNA Copy Number Variations<br/>DNA Mutational Analysis<br/>Exons--genetics<br/>Eye Abnormalities--genetics<br/>Eye Diseases, Hereditary<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Male<br/>Mutation<br/>Open Reading Frames--genetics<br/>Pedigree<br/>Real-Time Polymerase Chain Reaction<br/>Sequence Deletion<br/>Transcription Factors--genetics<br/>Homeobox Protein PITX2