Exclusion of non-synonymous SNPs and a polyglutamine tract in SMRT/N-CoR2 as common deleterious mutation for bipolar disorder in the Sagnenay-Lac-St-Jean population

American Journal of Medical Genetics - Neuropsychiatric Genetics

Volumn 134 B, Issue 1, 2005, Pages 10-12

  Shink, Eric ^a   Harvey, Mario ^a   Tremblay, Monique ^a   Raymond, Catherine ^a   Labbé, Michel ^a   Gagné, Bernard ^a   Barden, Nicholas ^a  

^a LAVAL UNIVERSITY   (Canada)

Author keywords

Anticipation; Bipolar disorder; Case control sample; Hypothalamic pituitary thyroid axis; SMRT N CoR2

Indexed keywords

NUCLEAR RECEPTOR COREPRESSOR; NUCLEAR RECEPTOR COREPRESSOR 2; POLYGLUTAMINE; THYROID HORMONE RECEPTOR; UNCLASSIFIED DRUG;

ADULT; ALLELIC IMBALANCE; ARTICLE; BIPOLAR DISORDER; CANADA; CHROMOSOME 12; CONTROLLED STUDY; CPG ISLAND; DNA POLYMORPHISM; EXON; FEMALE; GENE; GENE LOCUS; GENE MUTATION; GENETIC ASSOCIATION; GENETIC CODE; GENETIC LINKAGE; GENETIC SCREENING; GENETIC SUSCEPTIBILITY; HAPLOTYPE; HUMAN; INTRON; MAJOR CLINICAL STUDY; MALE; NUCLEOTIDE REPEAT; NUCLEOTIDE SEQUENCE; PHENOTYPE; POPULATION RESEARCH; PREVALENCE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SMRT GENE;

ALLELES; BIPOLAR DISORDER; DNA-BINDING PROTEINS; GENE FREQUENCY; GENOTYPE; GLUTAMINE; HAPLOTYPES; HUMANS; MUTATION; PEPTIDES; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; QUEBEC; REPRESSOR PROTEINS; TRINUCLEOTIDE REPEATS;

EID: 15744379462     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.30145     Document Type: Article

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