Moens, Lotte N <br/><br/>
Sequencing of DISC1 pathway genes reveals increased burden of rare missense variants in schizophrenia patients from a northern Swedish population.  [electronic resource] 

 -  PloS one  2011 
 - e23450 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1932-6203 
<br/><br/><label>Standard No.: </label>10.1371/journal.pone.0023450  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Case-Control Studies<br/>Computational Biology<br/>DNA Mutational Analysis<br/>Frameshift Mutation--genetics<br/>Gene Frequency--genetics<br/>Genetic Predisposition to Disease<br/>Genetics, Population<br/>Humans<br/>Middle Aged<br/>Mutation, Missense--genetics<br/>Nerve Tissue Proteins--genetics<br/>Reproducibility of Results<br/>Schizophrenia--epidemiology<br/>Sequence Analysis, DNA--methods<br/>Signal Transduction--genetics<br/>Sweden--epidemiology<br/>Young Adult