SLC25A12 and CMYA3 gene variants are not associated with autism in the IMGSAC multiplex family sample

European Journal of Human Genetics

Volumn 14, Issue 1, 2006, Pages 123-126

  Blasi, Francesca ^a,b,e   Bacchelli, Elena ^a,b   Carone, Simona ^a,b   Toma, Claudio ^a,b   Monaco, Anthony P ^c   Bailey, Anthony J ^d   Maestrini, Elena ^a,b  

^a UNIVERSITY OF BOLOGNA   (Italy)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c UNIVERSITY OF OXFORD   (United Kingdom)

^d Park Hospital for Children Oxford   (United Kingdom)

^e Dipartimento di Biologia Evoluzionistica Sperimentale   (Italy)

Author keywords

Association; Autism; Chromosome 2q; CMYA3; SLC25A12; SNPs

Indexed keywords

GENE PRODUCT; PROTEIN CMYA3; PROTEIN SLC25A12; UNCLASSIFIED DRUG;

ARTICLE; AUTISM; CASE CONTROL STUDY; CHROMOSOME 2Q; CONTROLLED STUDY; FAMILY; GENETIC ASSOCIATION; GENETIC PREDISPOSITION; GENETIC RISK; GENETIC SUSCEPTIBILITY; HUMAN; MAJOR CLINICAL STUDY; PRIORITY JOURNAL; SINGLE NUCLEOTIDE POLYMORPHISM;

AUTISTIC DISORDER; CASE-CONTROL STUDIES; DNA-BINDING PROTEINS; GENETIC PREDISPOSITION TO DISEASE; HAPLOTYPES; HUMANS; INTERNATIONAL COOPERATION; MEMBRANE TRANSPORT PROTEINS; MITOCHONDRIAL PROTEINS; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 29644444985     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201444     Document Type: Article

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