Erratum: Linkage and candidate gene studies of autism spectrum disorders in European populations (European Journal of Human Genetics (2010) 18 (1013-10190) DOI: 10.1038/ejhg.2010.69);Linkage and candidate gene studies of autism spectrum disorders in European populations

European Journal of Human Genetics

Volumn 18, Issue 9, 2010, Pages 1013-1020

  Holt, Richard ^a   Barnby, Gabrielle ^a   Maestrini, Elena ^b   Bacchelli, Elena ^b   Brocklebank, Denise ^a   Sousa, Iêns ^a   Mulder, Erik J ^c   Kantojärvi, Katri ^d   Järvelä, Irma ^d   Klauck, Sabine M ^e   Poustka, Fritz ^f   Bailey, Anthony J ^g   Monaco, Anthony P ^a  

^a UNIVERSITY OF OXFORD   (United Kingdom)

^b UNIVERSITY OF BOLOGNA   (Italy)

^c UNIVERSITY MEDICAL CENTER GRONINGEN   (Netherlands)

^d UNIVERSITY OF HELSINKI   (Finland)

^e GERMAN CANCER RESEARCH CENTER DKFZ   (Germany)

^f GOETHE UNIVERSITY   (Germany)

^g Park Hospital for Children Oxford   (United Kingdom)

Author keywords

association; autistic disorder; candidate gene; linkage

Indexed keywords

ACETYLSEROTONIN METHYLTRANSFERASE; PROTEIN KINASE C BETA; REELIN; SEROTONIN TRANSPORTER;

ARTICLE; AUTISM; CHROMOSOME 2; EUROPE; GENE; GENE LOCUS; GENE REPLICATION; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC SUSCEPTIBILITY; GENOMICS; GLUTAMATE RECEPTOR IONOTROPIC KAINITE 2 GENE; HUMAN; MYOCARDIN LIKE 2 GENE; NITRIC OXIDE SYNTHASE TRAFFICKER GENE; PRIORITY JOURNAL; SH3 AND MULTIPLE ANKYRIN REPEAT DOMAIN 3 GENE; SINGLE NUCLEOTIDE POLYMORPHISM; STAPHYLOCOCCAL NUCLEASE AND TUDOR DOMAIN CONTAINING 1 GENE;

EID: 77955981330     PISSN: 10184813     EISSN: 14765438     Source Type: Journal    
DOI: 10.1038/ejhg.2010.99     Document Type: Erratum

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