Strom, S P <br/><br/>
High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate gene.  [electronic resource] 

 -  Molecular psychiatry  Oct 2010 
 - 996-1005 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5578 
<br/><br/><label>Standard No.: </label>10.1038/mp.2009.41  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Autistic Disorder--epidemiology<br/>Calcium Channels, T-Type--genetics<br/>Child<br/>Chromosomes, Human, Pair 17<br/>Female<br/>Follow-Up Studies<br/>Gene Dosage<br/>Genetic Markers<br/>Genetic Predisposition to Disease--epidemiology<br/>Haplotypes<br/>Humans<br/>Linkage Disequilibrium<br/>Lod Score<br/>Male<br/>Polymorphism, Single Nucleotide<br/>Risk Factors