|  Help  |  About  |  Contact Us

Publication : UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis.

First Author  Daoud H Year  2012
Journal  Neurobiol Aging Volume  33
Issue  9 Pages  2230.e1-2230.e5
PubMed ID  22560112 Mgi Id 
Quick Links:
 
Quick Links:
 

Expression

Publication --> Expression annotations

 

Other

1 Bio Entities

Trail: Publication

0 Expression