Vernau, Karen M <br/><br/>
Genome-wide association analysis identifies a mutation in the thiamine transporter 2 (SLC19A3) gene associated with Alaskan Husky encephalopathy.  [electronic resource] 

 -  PloS one  2013 
 - e57195 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.0057195  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Animals<br/>Base Sequence<br/>Biological Transport--genetics<br/>Brain Diseases, Metabolic--genetics<br/>Dog Diseases--genetics<br/>Dogs<br/>Exons<br/>Female<br/>Genetic Loci<br/>Genome-Wide Association Study<br/>Heterozygote<br/>Homozygote<br/>Humans<br/>Leigh Disease--genetics<br/>Male<br/>Membrane Transport Proteins--genetics<br/>Molecular Sequence Data<br/>Mutation<br/>Polymorphism, Single Nucleotide<br/>Thiamine--metabolism