Association of DRD2 variants and Gilles de la Tourette syndrome in a family-based sample from a South American population isolate

Psychiatric Genetics

Volumn 20, Issue 4, 2010, Pages 179-183

  Herzberg, Ibi ^a   Valencia Duarte, Ana Victoria ^b   Kay, Victoria A ^a   White, Daniel J ^a   Müller, Heike ^a   Rivas, Isabel C ^c   Mesa, Sandra Catalina ^c   Cuartas, Mauricio ^b   García, Jharley ^b   Bedoya, Gabriel ^b   Cornejo, William ^c   Ruiz Linares, Andrés ^a,b   Kremeyer, Barbara ^a  

^a UNIVERSITY COLLEGE LONDON   (United Kingdom)

^b Laboratorio de Genética Molecular   (Spain)

^c UNIVERSIDAD DE ANTIOQUIA   (Colombia)

Author keywords

Association analysis; dopamine receptor D2 gene; population isolate; Tourette syndrome

Indexed keywords

DOPAMINE 2 RECEPTOR;

ARTICLE; COLOMBIA; DISEASE ASSOCIATION; DISEASE PREDISPOSITION; DOPAMINERGIC SYSTEM; FEMALE; GENETIC ANALYSIS; GENETIC RISK; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; NUCLEAR FAMILY; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; CHILD; FAMILY; GENE LINKAGE DISEQUILIBRIUM; GENE LOCUS; GENETIC PREDISPOSITION; GENETICS; MUTATION; SOUTH AMERICA;

CHILD; FAMILY; FEMALE; GENETIC LOCI; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; MUTATION; POLYMORPHISM, SINGLE NUCLEOTIDE; RECEPTORS, DOPAMINE D2; SOUTH AMERICA; TOURETTE SYNDROME;

EID: 77954888136     PISSN: 09558829     EISSN: None     Source Type: Journal    
DOI: 10.1097/YPG.0b013e32833a215a     Document Type: Article

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