Genetic analysis of SIGMAR1 as a cause of familial ALS with dementia

European Journal of Human Genetics

Volumn 21, Issue 2, 2013, Pages 237-239

  Belzil, Véronique V ^a   Daoud, Hussein ^a   Camu, William ^b   Strong, Michael J ^c   Dion, Patrick A ^a,d   Rouleau, Guy A ^a,d,e  

^a CENTRE HOSPITALIER DE L UNIVERSITÉ DE MONTRÉAL   (Canada)

^b GUI DE CHAULIAC HOSPITAL   (France)

^c UNIVERSITY OF WESTERN ONTARIO   (Canada)

^d UNIVERSITÉ DE MONTRÉAL   (Canada)

^e UNIVERSITY OF MONTREAL   (Canada)

Author keywords

Amyotrophic lateral sclerosis; dementia; frontotemporal lobar degeneration; motor neuron disease

Indexed keywords

3' UNTRANSLATED REGION; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; CAUCASIAN; CHROMOSOME; CLINICAL ARTICLE; COGNITIVE DEFECT; CONTROLLED STUDY; DEMENTIA; FAMILIAL DISEASE; GENE; GENE SEQUENCE; GENETIC ANALYSIS; GENETIC CODE; GENETIC SCREENING; GENETIC VARIABILITY; HUMAN; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SIGMAR1 GENE;

3' UNTRANSLATED REGIONS; AMYOTROPHIC LATERAL SCLEROSIS; DEMENTIA; DNA REPEAT EXPANSION; DNA-BINDING PROTEINS; FRONTOTEMPORAL LOBAR DEGENERATION; HUMANS; MOTOR NEURONS; PROTEINS; RECEPTORS, SIGMA; RNA-BINDING PROTEIN FUS;

EID: 84872493515     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2012.135     Document Type: Article

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