Kumar, Ravinesh A <br/><br/>
A de novo 1p34.2 microdeletion identifies the synaptic vesicle gene RIMS3 as a novel candidate for autism.  [electronic resource] 

 -  Journal of medical genetics  Feb 2010 
 - 81-90 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, N.I.H., Extramural 
<br/><br/><label>ISSN: </label>1468-6244 
<br/><br/><label>Standard No.: </label>10.1136/jmg.2008.065821  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Substitution<br/>Autistic Disorder--genetics<br/>Child<br/>Child, Preschool<br/>Comparative Genomic Hybridization<br/>DNA Mutational Analysis<br/>Databases, Genetic<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Male<br/>Membrane Transport Proteins--genetics<br/>Mutation, Missense<br/>Nerve Tissue Proteins--genetics<br/>Sequence Deletion