Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients

Neurobiology of Aging

Volumn 34, Issue 5, 2013, Pages 1516.e1-1516.e8

  Alavi, Afagh ^a   Nafissi, Shahriar ^b   Rohani, Mohammad ^b   Zamani, Babak ^b   Sedighi, Behnaz ^c   Shamshiri, Hosein ^b   Fan, Jian Bing ^d   Ronaghi, Mostafa ^d   Elahi, Elahe ^a  

^a UNIVERSITY OF TEHRAN   (Iran)

^b TEHRAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^c KERMAN UNIVERSITY OF MEDICAL SCIENCES   (Iran)

^d ILLUMINA INC   (United States)

Author keywords

ALS; Amyotrophic lateral sclerosis; Iran; P.Asp90Ala; P.D90A; Scandinavian haplotype; SOD1

Indexed keywords

COPPER ZINC SUPEROXIDE DISMUTASE;

ADOLESCENT; ADULT; AGED; ALLELE; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; COHORT ANALYSIS; FEMALE; GENE IDENTIFICATION; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC SCREENING; HOMOZYGOSITY; HUMAN; IRAN; LINKAGE ANALYSIS; MAJOR CLINICAL STUDY; MALE; MUTATIONAL ANALYSIS; NUCLEOTIDE SEQUENCE; PHENOTYPE; PRIORITY JOURNAL; SUPEROXIDE DISMUTASE 1 GENE;

EID: 84873430272     PISSN: 01974580     EISSN: 15581497     Source Type: Journal    
DOI: 10.1016/j.neurobiolaging.2012.09.006     Document Type: Article

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