Genome-wide association reveals three SNPs associated with sporadic amyotrophic lateral sclerosis through a two-locus analysis.

BMC medical genetics

Volumn 10, Issue , 2009, Pages 86-

  Sha, Qiuying ^a   Zhang, Zhaogong ^a   Schymick, Jennifer C ^a   Traynor, Bryan J ^a   Zhang, Shuanglin ^a  

^a MICHIGAN TECHNOLOGICAL UNIVERSITY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALLELE; AMYOTROPHIC LATERAL SCLEROSIS; ARTICLE; BIOLOGICAL MODEL; CASE CONTROL STUDY; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; HUMAN; RISK; SINGLE NUCLEOTIDE POLYMORPHISM; STATISTICAL MODEL;

ALLELES; AMYOTROPHIC LATERAL SCLEROSIS; CASE-CONTROL STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOME-WIDE ASSOCIATION STUDY; HUMANS; LIKELIHOOD FUNCTIONS; MODELS, GENETIC; ODDS RATIO; POLYMORPHISM, SINGLE NUCLEOTIDE;

MLCS; MLOWN;

EID: 70349581644     PISSN: None     EISSN: 14712350     Source Type: Journal    
DOI: 10.1186/1471-2350-10-86     Document Type: Article

References (0)