Association of mouse Dlg4 (PSD-95) gene deletion and human DLG4 gene variation with phenotypes relevant to autism spectrum disorders and Williams' syndrome

American Journal of Psychiatry

Volumn 167, Issue 12, 2010, Pages 1508-1517

  Feyder, Michael ^a   Karlsson, Rose Marie ^a   Mathur, Poonam ^a   Lyman, Matthew ^a   Bock, Roland ^a   Momenan, Reza ^a   Munasinghe, Jeeva ^a   Scattoni, Maria Luisa ^a   Ihne, Jessica ^a   Camp, Marguerite ^a   Graybeal, Carolyn ^a   Strathdee, Douglas ^a   Begg, Alison ^a   Alvarez, Veronica A ^a   Kirsch, Peter ^a   Rietschel, Marcella ^a   Cichon, Sven ^a   Walter, Henrik ^a   Meyer Lindenberg, Andreas ^a   Grant, Seth G N ^a   Holmes, Andrew ^a   more..

^a NONE

Author keywords

[No Author keywords available]

Indexed keywords

POSTSYNAPTIC DENSITY PROTEIN 95;

AMYGDALOID NUCLEUS; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ANXIETY; ARTICLE; AUTISM; BEHAVIOR DISORDER; BRAIN CORTEX; COMMUNICATION DISORDER; COMPULSION; CONTROLLED STUDY; CYLN2 GENE; DENDRITIC SPINE; DLG4 GENE; EMOTION; GENE; GENE DELETION; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC VARIABILITY; HUMAN; MAJOR CLINICAL STUDY; MOTOR COORDINATION; MOUSE; NONHUMAN; PHENOTYPE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM; SOCIAL BEHAVIOR; STRESS; WILLIAMS BEUREN SYNDROME;

ADULT; AMYGDALA; ANIMALS; BEHAVIOR, ANIMAL; CHILD; CHILD DEVELOPMENT DISORDERS, PERVASIVE; DENDRITIC SPINES; DISEASE MODELS, ANIMAL; FEMALE; GENE DELETION; GENETIC VARIATION; HUMANS; INTRACELLULAR SIGNALING PEPTIDES AND PROTEINS; MALE; MEMBRANE PROTEINS; MICE; MICE, INBRED C57BL; MICE, KNOCKOUT; NERVE TISSUE PROTEINS; NEURAL PATHWAYS; PARIETAL LOBE; PHENOTYPE; POLYMORPHISM, SINGLE NUCLEOTIDE; PROSENCEPHALON; WILLIAMS SYNDROME;

EID: 78649753616     PISSN: 0002953X     EISSN: 15357228     Source Type: Journal    
DOI: 10.1176/appi.ajp.2010.10040484     Document Type: Article

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