Association between AVPR1A, DRD2, and ASPM and endophenotypes of communication disorders

Psychiatric genetics

Volumn 24, Issue 5, 2014, Pages 191-200

  Stein, Catherine M ^a   Truitt, Barbara ^a   Deng, Fenghua ^a   Ciesla, Allison A vrich ^a   Qiu, Feiyou ^a   Joseph, Peronne ^a   Raghavendra, Rekha ^a   Fondran, Jeremy ^a   Igo, Robert P ^a   Tag, Jessica ^a   Freebairn, Lisa ^a   Taylor, H Gerry ^a   Lewis, Barbara A ^a   Iyengar, Sudha K ^a  

^a CASE WESTERN RESERVE UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ASPM PROTEIN, HUMAN; DOPAMINE 2 RECEPTOR; DRD2 PROTEIN, HUMAN; NERVE PROTEIN; VASOPRESSIN RECEPTOR;

CHILD; COMMUNICATION DISORDER; ENDOPHENOTYPE; FEMALE; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETICS; HUMAN; LANGUAGE DISABILITY; MALE; PRESCHOOL CHILD; QUANTITATIVE TRAIT;

CHILD; CHILD, PRESCHOOL; COMMUNICATION DISORDERS; ENDOPHENOTYPES; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; HUMANS; LANGUAGE DISORDERS; LINKAGE DISEQUILIBRIUM; MALE; NERVE TISSUE PROTEINS; QUANTITATIVE TRAIT, HERITABLE; RECEPTORS, DOPAMINE D2; RECEPTORS, VASOPRESSIN;

EID: 85027946049     PISSN: None     EISSN: 14735873     Source Type: Journal    
DOI: 10.1097/YPG.0000000000000045     Document Type: Article

References (0)