Chograni, Mančl <br/><br/>
Absence of mutations in four genes encoding for congenital cataract and expressed in the human brain in Tunisian families with cataract and mental retardation.  [electronic resource] 

 -  BMC ophthalmology  Nov 2011 
 - 35 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1471-2415 
<br/><br/><label>Standard No.: </label>10.1186/1471-2415-11-35  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adolescent<br/>Adult<br/>Cataract--complications<br/>Child<br/>Consanguinity<br/>DNA Mutational Analysis<br/>DNA-Binding Proteins--genetics<br/>Eye Proteins--genetics<br/>Family<br/>Female<br/>Gene Frequency<br/>Heat Shock Transcription Factors<br/>Homeodomain Proteins--genetics<br/>Humans<br/>Intellectual Disability--complications<br/>Introns--genetics<br/>Male<br/>Membrane Proteins--genetics<br/>Microcephaly--genetics<br/>Mutation--genetics<br/>Transcription Factors--genetics<br/>Tunisia<br/>Young Adult