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Volumn 12, Issue 11 SUPPL., 2011, Pages

Potential genetic risk factors for chronic TMD: Genetic Associations from the OPPERA case control study

(14)  Smith, Shad B a   Maixner, Dylan W a   Greenspan, Joel D d   Dubner, Ronald d   Fillingim, Roger B e   Ohrbach, Richard f   Knott, Charles g   Slade, Gary D a,b   Bair, Eric a,b   Gibson, Dustin G a   Zaykin, Dmitri V h   Weir, Bruce S i   Maixner, William a,c   Diatchenko, Luda a,j  


Author keywords

association study; CAMK4; CHRM2; COMT; GRK5; HTR2A; IFRD1; NR3C1; Pain genetics; temporomandibular joint disorders (TMD)

Indexed keywords

ARTICLE; CHRONIC DISEASE; CONTROLLED STUDY; DISEASE CLASSIFICATION; ETHNICITY; FEMALE; GENE EXPRESSION; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC RISK; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MARKER GENE; MEDICAL RESEARCH; POPULATION GENETICS; RISK ASSESSMENT; SINGLE NUCLEOTIDE POLYMORPHISM; TEMPOROMANDIBULAR JOINT DISORDER;

EID: 80755169522     PISSN: 15265900     EISSN: 15288447     Source Type: Journal    
DOI: 10.1016/j.jpain.2011.08.005     Document Type: Article
Times cited : (161)

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