Tarlarini, C <br/><br/>
Novel FUS mutations identified through molecular screening in a large cohort of familial and sporadic amyotrophic lateral sclerosis.  [electronic resource] 

 -  European journal of neurology  Nov 2015 
 - 1474-81 p.  digital 
<br/><br/> Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1468-1331 
<br/><br/><label>Standard No.: </label>10.1111/ene.12772  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Amyotrophic Lateral Sclerosis--genetics<br/>Cohort Studies<br/>Exons<br/>Female<br/>Humans<br/>Italy<br/>Male<br/>Middle Aged<br/>Mutation<br/>RNA-Binding Protein FUS--genetics<br/>Sex Factors