Blauw, Hylke M <br/><br/>
A large genome scan for rare CNVs in amyotrophic lateral sclerosis.  [electronic resource] 

 -  Human molecular genetics  Oct 2010 
 - 4091-9 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1460-2083 
<br/><br/><label>Standard No.: </label>10.1093/hmg/ddq323  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Amyotrophic Lateral Sclerosis--genetics<br/>Case-Control Studies<br/>DNA Copy Number Variations<br/>Dipeptidyl-Peptidases and Tripeptidyl-Peptidases--genetics<br/>Genetic Predisposition to Disease<br/>Genetic Variation<br/>Genome, Human<br/>Genome-Wide Association Study<br/>Humans<br/>Membrane Proteins--genetics<br/>Motor Neurons<br/>Nerve Tissue Proteins--genetics<br/>Polymerase Chain Reaction<br/>Polymorphism, Single Nucleotide<br/>Potassium Channels--genetics<br/>Risk Factors<br/>Spastic Paraplegia, Hereditary--genetics