No association between common variations in the neuronal nicotinic acetylcholine receptor alpha2 subunit gene (CHRNA2) and bipolar I disorder

Psychiatry Research

Volumn 135, Issue 3, 2005, Pages 171-177

  Lohoff, Falk W ^a   Ferraro, Thomas N ^a   McNabb, Leilah ^a   Schwebel, Candice ^a   Dahl, John P ^a   Doyle, Glenn A ^a   Buono, Russell J ^a   Berrettini, Wade H ^a  

^a UNIVERSITY OF PENNSYLVANIA   (United States)

Author keywords

Association study; Chromosome 8p; Genetics; Polymorphism

Indexed keywords

NICOTINIC RECEPTOR; NICOTINIC RECEPTOR ALPHA2; UNCLASSIFIED DRUG;

AGE DISTRIBUTION; AMINO ACID SUBSTITUTION; ARTICLE; BIPOLAR I DISORDER; CONTROLLED STUDY; FEMALE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

BIPOLAR DISORDER; CASE-CONTROL STUDIES; CHROMOSOMES, HUMAN, PAIR 8; DIAGNOSTIC AND STATISTICAL MANUAL OF MENTAL DISORDERS; FEMALE; GENE FREQUENCY; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; POLYMORPHISM, GENETIC; RECEPTORS, NICOTINIC; TOBACCO USE DISORDER; VARIATION (GENETICS);

EID: 22144432954     PISSN: 01651781     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.psychres.2005.04.004     Document Type: Article

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