Family-based genetic association study of DLGAP3 in Tourette Syndrome

American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics

Volumn 156, Issue 1, 2011, Pages 108-114

  Crane, Jacquelyn ^a   Fagerness, Jesen ^a   Osiecki, Lisa ^a   Gunnell, Boyd ^a   Stewart, S Evelyn ^a,b   Pauls, David L ^a   Scharf, Jeremiah M ^a   Cath, D ^b,c   Heutink, P ^b,c   Grados, M ^b,d   Singer, H S ^b,d   Walkup, J T ^b,d   J M Scharf, ^a,b   Illmann, C ^a,b   Yu, D ^a,b   Platko, J ^a,b   Santangelo, S ^a,b   Pauls, D L ^a,b   Cox, N J ^b,e   Service, S ^b,f   Keen Kim, D ^b,f   Sabatti, C ^b,f   Freimer, N ^b,f   Robertson, M M ^b,g   Rouleau, G A ^b,h   Riviere, J B ^b,h   Chouinard, S ^b,h   Richer, F ^b,h   Lesperance, P ^b,h   Dion, Y ^b,h   King, R A ^b,i   Kidd, J R ^b,i   Pakstis, A J ^b,i   Leckman, J F ^b,i   Kidd, K K ^b,i   Kurlan, R ^b,j   Como, P ^b,j   Palumbo, D ^b,j   Verkerk, A ^b,k   Oostra, B A ^b,k   McMahon, W ^b,l   Leppert, M ^b,l   Coon, H ^b,l   Mathews, C ^b,m   Sandor, P ^b,n   Barr, C L ^b,n   more..

^a MASSACHUSETTS GENERAL HOSPITAL   (United States)

^b Tourette Syndrome Association   (United States)

^c VU UNIVERSITY MEDICAL CENTER   (Netherlands)

^d JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE   (United States)

^e UNIVERSITY OF CHICAGO   (United States)

^f UNIVERSITY OF CALIFORNIA   (United States)

^g NATIONAL HOSPITAL FOR NEUROLOGY AND NEUROSURGERY   (United Kingdom)

^h UNIVERSITÉ DE MONTRÉAL   (Canada)

ⁱ YALE UNIVERSITY SCHOOL OF MEDICINE   (United States)

^j UNIVERSITY OF ROCHESTER SCHOOL OF MEDICINE AND DENTISTRY   (United States)

^k ERASMUS UNIVERSITY ROTTERDAM   (Netherlands)

^l UNIVERSITY OF UTAH SCHOOL OF MEDICINE   (United States)

^m UNIVERSITY OF CALIFORNIA   (United States)

ⁿ UNIVERSITY HEALTH NETWORK   (Canada)

more..

Author keywords

Gene; Glutamate; SAPAP3; Tic disorders; Trichotillomania

Indexed keywords

POSTSYNAPTIC DENSITY PROTEIN 95; SAP90 PSD95 ASSOCIATED PROTEIN 3; SCAFFOLD PROTEIN; UNCLASSIFIED DRUG; NERVE PROTEIN; SAPAP3 PROTEIN, HUMAN;

ALLELE; ARTICLE; COMORBIDITY; FAMILIAL DISEASE; FAMILY; GENE FREQUENCY; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; GILLES DE LA TOURETTE SYNDROME; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; GENE LINKAGE DISEQUILIBRIUM; GENETIC MARKER; GENETICS;

FAMILY; GENETIC ASSOCIATION STUDIES; GENETIC MARKERS; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; NERVE TISSUE PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; TOURETTE SYNDROME;

EID: 79952243302     PISSN: 15524841     EISSN: 1552485X     Source Type: Journal    
DOI: 10.1002/ajmg.b.31134     Document Type: Article

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