Rare missense neuronal cadherin gene (CDH2) variants in specific obsessive-compulsive disorder and Tourette disorder phenotypes

European Journal of Human Genetics

Volumn 21, Issue 8, 2013, Pages 850-854

  Moya, Pablo R ^a   Dodman, Nicholas H ^b   Timpano, Kiara R ^c   Rubenstein, Liza M ^a   Rana, Zaker ^a   Fried, Ruby L ^a   Reichardt, Louis F ^d   Heiman, Gary A ^e   Tischfield, Jay A ^e   King, Robert A ^f   Galdzicka, Marzena ^g   Ginns, Edward I ^g   Wendland, Jens R ^h  

^a NATIONAL INSTITUTE OF MENTAL HEALTH   (United States)

^b TUFTS UNIVERSITY   (United States)

^c UNIVERSITY OF MIAMI   (United States)

^d UNIVERSITY OF CALIFORNIA   (United States)

^e Life Sciences Building Rutgers University   (United States)

^f YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^g UNIVERSITY OF MASSACHUSETTS MEDICAL SCHOOL   (United States)

^h F HOFFMANN LA ROCHE LTD   (Switzerland)

Author keywords

Canine compulsive disorder; CDH2; N cadherin; Obsessive compulsive disorder; Rare gene variants; Tourette disorder

Indexed keywords

CADHERIN;

ARTICLE; AUTISM; CELL ADHESION; CLINICAL FEATURE; CONTROLLED STUDY; DISEASE SEVERITY; EXON; GENE SEQUENCE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; GILLES DE LA TOURETTE SYNDROME; HUMAN; MAJOR CLINICAL STUDY; MISSENSE MUTATION; OBSESSIVE COMPULSIVE DISORDER; PHENOTYPE; PRIORITY JOURNAL; PROTEIN EXPRESSION; SINGLE NUCLEOTIDE POLYMORPHISM;

ADULT; ANTIGENS, CD; BLOTTING, WESTERN; CADHERINS; DNA MUTATIONAL ANALYSIS; GENOTYPE; HEK293 CELLS; HUMANS; MUTATION, MISSENSE; OBSESSIVE-COMPULSIVE DISORDER; PHENOTYPE; PSYCHIATRIC STATUS RATING SCALES; TOURETTE SYNDROME; TRANSFECTION;

EID: 84880918447     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2012.245     Document Type: Article

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