Seelen, Meinie <br/><br/>
No mutations in hnRNPA1 and hnRNPA2B1 in Dutch patients with amyotrophic lateral sclerosis, frontotemporal dementia, and inclusion body myopathy.  [electronic resource] 

 -  Neurobiology of aging  Aug 2014 
 - 1956.e9-1956.e11 p.  digital 
<br/><br/> Publication Type: Journal Article; Research Support, Non-U.S. Gov't 
<br/><br/><label>ISSN: </label>1558-1497 
<br/><br/><label>Standard No.: </label>10.1016/j.neurobiolaging.2014.01.152  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Adult<br/>Aged<br/>Aged, 80 and over<br/>Amyotrophic Lateral Sclerosis--genetics<br/>Cohort Studies<br/>Female<br/>Frontotemporal Dementia--genetics<br/>Genetic Association Studies<br/>Heterogeneous Nuclear Ribonucleoprotein A1<br/>Heterogeneous-Nuclear Ribonucleoprotein Group A-B--genetics<br/>Humans<br/>Male<br/>Middle Aged<br/>Mutation<br/>Myositis, Inclusion Body--genetics<br/>Netherlands<br/>Osteitis Deformans--genetics