Converging evidence for an association of ATP2B2 allelic variants with autism in male subjects

Biological Psychiatry

Volumn 70, Issue 9, 2011, Pages 880-887

  Carayol, Jérme ^a   Sacco, Roberto ^b,c   Tores, Frédéric ^a   Rousseau, Francis ^a   Lewin, Patricia ^a   Hager, Jorg ^a   Persico, Antonio M ^b,c  

^a CEA Fontenay aux Roses Bâtiment 61   (France)

^b UNIVERSITY CAMPUS BIO MEDICO   (Italy)

^c IRCCS FONDAZIONE SANTA LUCIA   (Italy)

Author keywords

ATP2B2; autistic disorder; calcium; gender heterogeneity; pervasive developmental disorders; PMCA2

Indexed keywords

ALLELE; ARTICLE; ATP2B2 GENE; AUTISM; EXON; FEMALE; GENE; GENE FREQUENCY; GENE LINKAGE DISEQUILIBRIUM; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC VARIABILITY; GENOTYPE; HUMAN; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

ALGORITHMS; ALLELES; AUTISTIC DISORDER; DNA REPLICATION; FAMILY; FEMALE; GENES, RECESSIVE; GENETIC MARKERS; GENETIC VARIATION; GENOME-WIDE ASSOCIATION STUDY; GENOTYPE; HUMANS; INTELLIGENCE TESTS; ITALY; LINKAGE DISEQUILIBRIUM; MALE; MODELS, GENETIC; PLASMA MEMBRANE CALCIUM-TRANSPORTING ATPASES; POLYMORPHISM, SINGLE NUCLEOTIDE; PSYCHIATRIC STATUS RATING SCALES;

EID: 79960261603     PISSN: 00063223     EISSN: 18732402     Source Type: Journal    
DOI: 10.1016/j.biopsych.2011.05.020     Document Type: Article

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