Petek, Erwin <br/><br/>
Molecular and genomic studies of IMMP2L and mutation screening in autism and Tourette syndrome.  [electronic resource] 

 -  Molecular genetics and genomics : MGG  Jan 2007 
 - 71-81 p.  digital 
<br/><br/> Publication Type: Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1617-4615 
<br/><br/><label>Standard No.: </label>10.1007/s00438-006-0173-1  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--genetics<br/>Cell Line<br/>Chromosomes, Human, Pair 7--genetics<br/>DNA Mutational Analysis<br/>Endopeptidases--genetics<br/>Gene Duplication<br/>Gene Expression Regulation--genetics<br/>Genetic Predisposition to Disease<br/>Humans<br/>Hybridomas<br/>Mutation<br/>Quantitative Trait Loci<br/>Tourette Syndrome--genetics