Piton, Amélie <br/><br/>
20 ans après: a second mutation in MAOA identified by targeted high-throughput sequencing in a family with altered behavior and cognition.  [electronic resource] 

 -  European journal of human genetics : EJHG  Jun 2014 
 - 776-83 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1476-5438 
<br/><br/><label>Standard No.: </label>10.1038/ejhg.2013.243  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amino Acid Sequence<br/>Attention Deficit and Disruptive Behavior Disorders--genetics<br/>Base Sequence<br/>Child Development Disorders, Pervasive--genetics<br/>Family Health<br/>Female<br/>Genetic Predisposition to Disease--genetics<br/>High-Throughput Nucleotide Sequencing--methods<br/>Humans<br/>Intellectual Disability--genetics<br/>Male<br/>Models, Molecular<br/>Monoamine Oxidase--chemistry<br/>Mutation, Missense<br/>Pedigree<br/>Protein Structure, Tertiary