Genetic Epidemiology, Translational Neurogenomics, Psychiatric Genetics and Statistical Genetics Laboratories investigate the pattern of disease in families, particularly identical and non-identical twins, to assess the relative importance of genes and environment in a variety of important health problems.
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PMID
19901951
TITLE
Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation.
ABSTRACT
DATE PUBLISHED
2010 Dec
HISTORY
PUBSTATUS PUBSTATUSDATE
aheadofprint 2009/11/10
entrez 2009/11/11 06:00
pubmed 2009/11/11 06:00
medline 2011/05/03 06:00
AUTHORS
NAME COLLECTIVENAME LASTNAME FORENAME INITIALS AFFILIATION AFFILIATIONINFO
Bates TC Department of Psychology, University of Edinburgh, Edinburgh, UK. tim.bates@ed.ac.uk
Lind PA
Luciano M
Montgomery GW
Martin NG
Wright MJ
INVESTIGATORS
JOURNAL
MEDLINE JOURNAL
MEDLINETA: Mol Psychiatry
COUNTRY: England
ISSNLINKING: 1359-4184
NLMUNIQUEID: 9607835
PUBLICATION TYPE
PUBLICATIONTYPE TEXT
Journal Article
Research Support, Non-U.S. Gov't
Twin Study
COMMENTS AND CORRECTIONS
GRANTS
GRANTID AGENCY COUNTRY
CZB/4/536 Chief Scientist Office United Kingdom
Chief Scientist Office United Kingdom
GENERAL NOTE
KEYWORDS
MESH HEADINGS
DESCRIPTORNAME QUALIFIERNAME
Adolescent
Adult
Child
Diseases in Twins genetics
Dyslexia genetics
Female genetics
Genetic Predisposition to Disease genetics
Humans genetics
Male genetics
Memory, Short-Term physiology
Mutation, Missense physiology
Nerve Tissue Proteins genetics
Nuclear Proteins genetics
Polymorphism, Single Nucleotide genetics
Reading genetics
Twins, Dizygotic genetics
Twins, Monozygotic genetics
Verbal Behavior physiology
Young Adult physiology
SUPPLEMENTARY MESH
GENE SYMBOLS
CHEMICALS
REGISTRYNUMBER NAMEOFSUBSTANCE
0 DYX1C1 protein, human
0 Nerve Tissue Proteins
0 Nuclear Proteins
OTHER ID's