Dyslexia and DYX1C1: Deficits in reading and spelling associated with a missense mutation

Molecular Psychiatry

Volumn 15, Issue 12, 2010, Pages 1190-1196

  Bates, T C ^a,b   Lind, P A ^b   Luciano, M ^a,b   Montgomery, G W ^b   Martin, N G ^b   Wright, M J ^b  

^a UNIVERSITY OF EDINBURGH   (United Kingdom)

^b QIMR BERGHOFER MEDICAL RESEARCH INSTITUTE   (Australia)

Author keywords

association; dyslexia; DYX1C1; family based; reading ability; spelling ability

Indexed keywords

ADOLESCENT; ADULT; ARTICLE; CHILD; DYSLEXIA; DYX1C1 GENE; FEMALE; GENETIC ASSOCIATION; GENETIC SUSCEPTIBILITY; HUMAN; LANGUAGE DISABILITY; MAJOR CLINICAL STUDY; MALE; MISSENSE MUTATION; PRIORITY JOURNAL; READING; SCHOOL CHILD; SHORT TERM MEMORY; SINGLE NUCLEOTIDE POLYMORPHISM; SPELLING;

ADOLESCENT; ADULT; CHILD; DISEASES IN TWINS; DYSLEXIA; FEMALE; GENETIC PREDISPOSITION TO DISEASE; HUMANS; MALE; MEMORY, SHORT-TERM; MUTATION, MISSENSE; NERVE TISSUE PROTEINS; NUCLEAR PROTEINS; POLYMORPHISM, SINGLE NUCLEOTIDE; READING; TWINS, DIZYGOTIC; TWINS, MONOZYGOTIC; VERBAL BEHAVIOR; YOUNG ADULT;

EID: 78650241792     PISSN: 13594184     EISSN: 14765578     Source Type: Journal    
DOI: 10.1038/mp.2009.120     Document Type: Article

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