Schizophrenia related variants in CACNA1C also confer risk of autism

PLoS ONE

Volumn 10, Issue 7, 2015, Pages

  Li, Jun ^a,b   Zhao, Linnan ^a,b   You, Yang ^a,b   Lu, Tianlan ^a,b   Jia, Meixiang ^a,b   Yu, Hao ^a,b,c   Ruan, Yanyan ^a,b   Yue, Weihua ^a,b   Liu, Jing ^a,b   Lu, Lin ^a,b   Zhang, Dai ^a,b,c   Wang, Lifang ^a,b  

^a PEKING UNIVERSITY SIXTH HOSPITAL   (China)

^b PEKING UNIVERSITY   (China)

^c Tsinghua University   (China)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ARTICLE; AUTISM; CACNA1C GENE; CHILD; CONTROLLED STUDY; FEMALE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENETIC ASSOCIATION; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENETIC VARIABILITY; GENOTYPE; HAN CHINESE; HAPLOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; MENTAL DISEASE; MINOR ALLELE FREQUENCY; MUTATIONAL ANALYSIS; PATHOGENESIS; SCHIZOPHRENIA; SINGLE NUCLEOTIDE POLYMORPHISM; TIMOTHY SYNDROME; TREND STUDY; ALLELE; ASIAN CONTINENTAL ANCESTRY GROUP; CHINA; GENETIC ASSOCIATION STUDY; GENETIC PREDISPOSITION; GENETICS; PRESCHOOL CHILD;

CACNA1C PROTEIN, HUMAN; CALCIUM CHANNEL L TYPE;

ADOLESCENT; ALLELES; ASIAN CONTINENTAL ANCESTRY GROUP; AUTISM SPECTRUM DISORDER; CALCIUM CHANNELS, L-TYPE; CHILD; CHILD, PRESCHOOL; CHINA; FEMALE; GENETIC ASSOCIATION STUDIES; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; MALE; POLYMORPHISM, SINGLE NUCLEOTIDE; SCHIZOPHRENIA;

EID: 84941670441     PISSN: None     EISSN: 19326203     Source Type: Journal    
DOI: 10.1371/journal.pone.0133247     Document Type: Article

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