Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.
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A missense mutation in DCDC2 causes human recessive deafness DFNB66, likely by interfering with sensory hair cell and supporting cell cilia length regulationThe regulatory element READ1 epistatically influences reading and language, with both deleterious and protective alleles.Dyslexia and language impairment associated genetic markers influence cortical thickness and white matter in typically developing childrenGray Matter Features of Reading Disability: A Combined Meta-Analytic and Direct Analysis Approach(1,2,3,4).Imaging-genetics in dyslexia: connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments.Mutation of Dcdc2 in mice leads to impairments in auditory processing and memory ability.Characterization of the DYX2 locus on chromosome 6p22 with reading disability, language impairment, and IQNeurogenetics of developmental dyslexia: from genes to behavior through brain neuroimaging and cognitive and sensorial mechanismsRet finger protein-like 3 promotes tumor cell growth by activating telomerase reverse transcriptase expression in human lung cancer cellsThe DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexia.The DYX2 locus and neurochemical signaling genes contribute to speech sound disorder and related neurocognitive domainsStrong motion deficits in dyslexia associated with DCDC2 gene alteration.Genome-wide association study of shared components of reading disability and language impairment.DCDC2 gene polymorphisms are associated with developmental dyslexia in Chinese Uyghur children.Molecular genetics of dyslexia: an overview.Disruption of long-range gene regulation in human genetic disease: a kaleidoscope of general principles, diverse mechanisms and unique phenotypic consequences.The DCDC2 deletion is not a risk factor for dyslexiaTranslating dyslexia across species.Study of Genetic Association With DCDC2 and Developmental Dyslexia in Hong Kong Chinese Children.Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNC.The role of READ1 and KIAA0319 genetic variations in developmental dyslexia: testing main and interactive effects.Visual motion and rapid auditory processing are solid endophenotypes of developmental dyslexia.The role of DCDC2 genetic variants and low socioeconomic status in vulnerability to attention problems.Complex effects of dyslexia risk factors account for ADHD traits: evidence from two independent samples.Association study of developmental dyslexia candidate genes DCDC2 and KIAA0319 in Chinese population.An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.The DCDC2 intron 2 deletion impairs illusory motion perception unveiling the selective role of magnocellular-dorsal stream in reading (dis)ability.Worldwide distribution of the DCDC2 READ1 regulatory element and its relationship with phoneme variation across languages.The interface between genetics and psychology: lessons from developmental dyslexia.
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Alleles of a polymorphic ETV6 binding site in DCDC2 confer risk of reading and language impairment.
description
article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on 06 June 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Alleles of a polymorphic ETV6 ...... ading and language impairment.
@en
Alleles of a polymorphic ETV6 ...... ading and language impairment.
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type
label
Alleles of a polymorphic ETV6 ...... ading and language impairment.
@en
Alleles of a polymorphic ETV6 ...... ading and language impairment.
@nl
prefLabel
Alleles of a polymorphic ETV6 ...... ading and language impairment.
@en
Alleles of a polymorphic ETV6 ...... ading and language impairment.
@nl
P2093
P2860
P50
P1476
Alleles of a polymorphic ETV6 ...... ading and language impairment.
@en
P2093
Jeffrey R Gruen
John D Eicher
Laura L Miller
Matthias Mann
Susan M Ring
P2860
P356
10.1016/J.AJHG.2013.05.008
P407
P577
2013-06-06T00:00:00Z