A rare WNT1 missense variant overrepresented in ASD leads to increased Wnt signal pathway activation.

Translational psychiatry

Volumn 3, Issue , 2013, Pages

  Martin, P M ^a   Yang, X ^b   Robin, N ^b   Lam, E ^b   Rabinowitz, J S ^b   Erdman, C A ^b   Quinn, J ^b   Weiss, L A ^b   Hamilton, S P ^b   Kwok, P Y ^b   Moon, R T ^b   Cheyette, B N ^b  

^a UNIVERSITY OF CALIFORNIA   (United States)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

WNT1 PROTEIN; WNT1 PROTEIN, HUMAN;

ARTICLE; AUTISM; CASE CONTROL STUDY; GENE FREQUENCY; GENETICS; GENOTYPE; HUMAN; MISSENSE MUTATION; REVERSE TRANSCRIPTION POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION; SINGLE NUCLEOTIDE POLYMORPHISM; WNT SIGNALING PATHWAY;

CASE-CONTROL STUDIES; CHILD DEVELOPMENT DISORDERS, PERVASIVE; GENE FREQUENCY; GENOTYPE; HUMANS; MUTATION, MISSENSE; POLYMORPHISM, SINGLE NUCLEOTIDE; REVERSE TRANSCRIPTASE POLYMERASE CHAIN REACTION; SIGNAL TRANSDUCTION; WNT SIGNALING PATHWAY; WNT1 PROTEIN;

EID: 84901884701     PISSN: None     EISSN: 21583188     Source Type: Journal    
DOI: 10.1038/tp.2013.75     Document Type: Article

References (0)