Willsey, A Jeremy <br/><br/>
De Novo Coding Variants Are Strongly Associated with Tourette Disorder.  [electronic resource] 

 -  Neuron  May 2017 
 - 486-499.e9 p.  digital 
<br/><br/> Publication Type: Journal Article; Video-Audio Media 
<br/><br/><label>ISSN: </label>1097-4199 
<br/><br/><label>Standard No.: </label>10.1016/j.neuron.2017.04.024  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Cadherins--genetics<br/>Cell Cycle Proteins<br/>Child<br/>Cohort Studies<br/>Female<br/>Fibronectins--genetics<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Humans<br/>Intracellular Signaling Peptides and Proteins--genetics<br/>Male<br/>Mutation<br/>Odds Ratio<br/>Parents<br/>Phosphoproteins--genetics<br/>Proteins--genetics<br/>Receptors, Cell Surface--genetics<br/>Sequence Analysis, DNA<br/>Tourette Syndrome--genetics