TY  - GEN
AU  - Daoud,Hussein
AU  - Suhail,Hamid
AU  - Szuto,Anna
AU  - Camu,William
AU  - Salachas,Francois
AU  - Meininger,Vincent
AU  - Bouchard,Jean-Pierre
AU  - Dupré,Nicolas
AU  - Dion,Patrick A
AU  - Rouleau,Guy A
TI  - UBQLN2 mutations are rare in French and French-Canadian amyotrophic lateral sclerosis
SN  - 1558-1497
PY  - 2012///1129
KW  - Adaptor Proteins, Signal Transducing
KW  - Amyotrophic Lateral Sclerosis
KW  - genetics
KW  - Animals
KW  - Autophagy-Related Proteins
KW  - Canada
KW  - Cell Cycle Proteins
KW  - Computational Biology
KW  - DNA Mutational Analysis
KW  - Female
KW  - Genetic Predisposition to Disease
KW  - Humans
KW  - Male
KW  - Mutation, Missense
KW  - Ubiquitins
KW  - White People
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/j.neurobiolaging.2012.03.015
ER  -