Family-based association study of DYX1C1 variants in autism

European Journal of Human Genetics

Volumn 13, Issue 1, 2005, Pages 127-130

  Ylisaukko Oja, Tero ^a,b   Peyrard Janvid, Myriam ^c   Lindgren, Cecilia M ^c   Rehnström, Karola ^a,b   Vanhala, Raija ^d   Peltonen, Leena ^a   Järvelä, Irma ^b,e   Kere, Juha ^b,c  

^a NATIONAL PUBLIC HEALTH INSTITUTE   (Finland)

^b UNIVERSITY OF HELSINKI   (Finland)

^c KAROLINSKA INSTITUTE   (Sweden)

^d HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

^e HELSINKI UNIVERSITY CENTRAL HOSPITAL   (Finland)

Author keywords

15q; Dyslexia; DYX1; FBAT; Hyperlexia; Specific language impairment

Indexed keywords

PROTEIN DYX1C1; TETRATRICOPEPTIDE REPEAT PROTEIN; UNCLASSIFIED DRUG;

ALLELE; ARTICLE; AUTISM; CHROMOSOME 15Q; COMORBIDITY; DISEASE ASSOCIATION; DYSLEXIA; EDUCATION; FAMILY STUDY; FINLAND; GENETIC VARIABILITY; HAPLOTYPE; HUMAN; INTELLIGENCE; LANGUAGE DEVELOPMENT; LEARNING DISORDER; MOTIVATION; PHENOTYPE; PRIORITY JOURNAL; PROTEIN VARIANT; READING; RISK ASSESSMENT; WRITING;

ALLELES; AUTISTIC DISORDER; FAMILY; FEMALE; GENETIC MARKERS; GENETIC PREDISPOSITION TO DISEASE; GENOTYPE; HAPLOTYPES; HUMANS; LINKAGE DISEQUILIBRIUM; MALE; NERVE TISSUE PROTEINS; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE;

EID: 12744274791     PISSN: 10184813     EISSN: None     Source Type: Journal    
DOI: 10.1038/sj.ejhg.5201272     Document Type: Article

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