Schormair, B <br/><br/>
Diagnostic exome sequencing in early-onset Parkinson's disease confirms VPS13C as a rare cause of autosomal-recessive Parkinson's disease.  [electronic resource] 

 -  Clinical genetics  03 2018 
 - 603-612 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1399-0004 
<br/><br/><label>Standard No.: </label>10.1111/cge.13124  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Age of Onset<br/>Alleles<br/>DNA Mutational Analysis<br/>Female<br/>Genes, Recessive<br/>Genetic Association Studies--methods<br/>Genetic Predisposition to Disease<br/>Genetic Testing<br/>Genotype<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Parkinson Disease--diagnosis<br/>Pedigree<br/>Proteins--genetics<br/>Risk Factors<br/>Sequence Analysis, DNA<br/>Exome Sequencing--methods<br/>Young Adult