Vilariño-Güell, Carles <br/><br/>
Exome sequencing in multiple sclerosis families identifies 12 candidate genes and nominates biological pathways for the genesis of disease.  [electronic resource] 

 -  PLoS genetics  06 2019 
 - e1008180 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1553-7404 
<br/><br/><label>Standard No.: </label>10.1371/journal.pgen.1008180  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Codon, Nonsense<br/>Demyelinating Diseases--genetics<br/>Exome--genetics<br/>Female<br/>Genetic Predisposition to Disease<br/>Humans<br/>Inflammation--genetics<br/>Male<br/>Middle Aged<br/>Multiple Sclerosis--genetics<br/>Myelin Sheath--genetics<br/>Nerve Degeneration--genetics<br/>Neurons--metabolism<br/>Pedigree<br/>Transcriptome--genetics<br/>Exome Sequencing<br/>Young Adult