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

Daoud, Hussein

UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis. [electronic resource] - Neurobiology of aging Sep 2012 - 2230.e1-2230.e5 p. digital

Publication Type: Journal Article; Research Support, Non-U.S. Gov't

1558-1497

10.1016/j.neurobiolaging.2012.03.015 doi


Adaptor Proteins, Signal Transducing
Amyotrophic Lateral Sclerosis--genetics
Animals
Autophagy-Related Proteins
Canada
Cell Cycle Proteins--genetics
Computational Biology
DNA Mutational Analysis
Female
Genetic Predisposition to Disease--genetics
Humans
Male
Mutation, Missense--genetics
Ubiquitins--genetics
White People--genetics