Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
about
Cellular function and pathological role of ATP13A2 and related P-type transport ATPases in Parkinson's disease and other neurological disordersAn examination of the language construct in NIMH's research domain criteria: Time for reconceptualization!Connecting the CNTNAP2 Networks with Neurodevelopmental DisordersIdentification and functional characterization of de novo FOXP1 variants provides novel insights into the etiology of neurodevelopmental disorderNeural FoxP2 and FoxP1 expression in the budgerigar, an avian species with adult vocal learningNormal radial migration and lamination are maintained in dyslexia-susceptibility candidate gene homolog Kiaa0319 knockout mice.A highly penetrant form of childhood apraxia of speech due to deletion of 16p11.2.Reading and language disorders: the importance of both quantity and quality.Monogenic and chromosomal causes of isolated speech and language impairment.Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech.Positive selection rather than relaxation of functional constraint drives the evolution of vision during chicken domestication.Bridging the Gap between Genes and Language Deficits in Schizophrenia: An Oscillopathic Approach.Insights into the genetic foundations of human communication.The role of candidate-gene CNTNAP2 in childhood apraxia of speech and specific language impairment.A Diagnostic Marker to Discriminate Childhood Apraxia of Speech From Speech Delay: I. Development and Description of the Pause Marker.Genome-Wide Studies of Specific Language Impairment.Prospective investigation of FOXP1 syndrome.Loss of Cntnap2 Causes Axonal Excitability Deficits, Developmental Delay in Cortical Myelination, and Abnormal Stereotyped Motor Behavior.Parkinson disease related ATP13A2 evolved early in animal evolution.CNTNAP2 Is Significantly Associated With Speech Sound Disorder in the Chinese Han Population.
P2860
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P2860
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
description
2013 nî lūn-bûn
@nan
2013 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի հոտեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
@nl
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@ast
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@en
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@en-gb
type
label
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
@nl
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@ast
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@en
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@en-gb
prefLabel
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
@nl
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@ast
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@en
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech.
@en-gb
P2093
P2860
P3181
P356
P1476
Whole-exome sequencing supports genetic heterogeneity in childhood apraxia of speech
@en
P2093
Edythe A Strand
Elizabeth A Worthey
Gordana Raca
Jennifer J Laffin
Jeremy M Harris
Kathy J Jakielski
Lawrence D Shriberg
P2860
P2888
P3181
P356
10.1186/1866-1955-5-29
P407
P577
2013-10-02T00:00:00Z
P5875
P6179
1048807461