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

Neurobiology of Aging

Volumn 33, Issue 9, 2012, Pages 2230.e1-2230.e5

  Daoud, Hussein ^a   Suhail, Hamid ^a   Szuto, Anna ^a   Camu, William ^b   Salachas, Francois ^c   Meininger, Vincent ^c   Bouchard, Jean Pierre ^d   Dupré, Nicolas ^d   Dion, Patrick A ^a,e   Rouleau, Guy A ^a,f  

^a UNIVERSITY OF MONTREAL   (Canada)

^b MONTPELLIER UNIVERSITY HOSPITAL   (France)

^c PITIÉ SALPÊTRIÈRE HOSPITAL   (France)

^d UNIVERSITÉ LAVAL   (Canada)

^e UNIVERSITÉ DE MONTRÉAL   (Canada)

^f UNIVERSITY OF MONTREAL   (Canada)

Author keywords

ALS; Dementia; UBQLN2

Indexed keywords

PROLINE; UBIQUILIN 2 PROTEIN; UBIQUITIN; UNCLASSIFIED DRUG;

AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; BIOINFORMATICS; CANADA; CONTROLLED STUDY; FRANCE; GENE FREQUENCY; GENE FUNCTION; GENE SEQUENCE; GENETIC ASSOCIATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MISSENSE MUTATION; MUTATIONAL ANALYSIS; MUTATOR GENE; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PRIORITY JOURNAL; PROTEIN DOMAIN; PROTEIN FUNCTION; STRUCTURE ANALYSIS; UBIQUILIN 2 GENE;

EID: 84863480094     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2012.03.015     Document Type: Article

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