The genetic basis of non-syndromic intellectual disability: a review
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Down Syndrome and Attention-Deficit/Hyperactivity Disorder (ADHD)De novo mutations in FOXP1 in cases with intellectual disability, autism, and language impairmentA circadian clock in hippocampus is regulated by interaction between oligophrenin-1 and Rev-erbαIntellectual disability associated with a homozygous missense mutation in THOC6The distinct and overlapping phenotypic spectra of FOXP1 and FOXP2 in cognitive disordersXLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencingFunction Over Form: Modeling Groups of Inherited Neurological Conditions in ZebrafishThe promise of multi-omics and clinical data integration to identify and target personalized healthcare approaches in autism spectrum disordersTruncation of the E3 ubiquitin ligase component FBXO31 causes non-syndromic autosomal recessive intellectual disability in a Pakistani familyExcess of de novo deleterious mutations in genes associated with glutamatergic systems in nonsyndromic intellectual disabilityMETTL23, a transcriptional partner of GABPA, is essential for human cognition.IL1RAPL1 knockout mice show spine density decrease, learning deficiency, hyperactivity and reduced anxiety-like behavioursLinks between mRNA splicing, mRNA quality control, and intellectual disabilityDisruption of the methyltransferase-like 23 gene METTL23 causes mild autosomal recessive intellectual disabilityIntellectual disability and autism spectrum disorders: causal genes and molecular mechanisms.Multilocus loss of DNA methylation in individuals with mutations in the histone H3 lysine 4 demethylase KDM5C.A defect in the CLIP1 gene (CLIP-170) can cause autosomal recessive intellectual disabilityMutations in the alpha 1,2-mannosidase gene, MAN1B1, cause autosomal-recessive intellectual disability.A New Role for LOC101928437 in Non-Syndromic Intellectual Disability: Findings from a Family-Based Association Test."Familial" versus "Sporadic" intellectual disability: contribution of common microdeletion and microduplication syndromesGenomic structural variants are linked with intellectual disability.Pulmonary lobectomies for patients with cognitive impairment: the importance of postoperative respiratory care.Mutation in NSUN2, which encodes an RNA methyltransferase, causes autosomal-recessive intellectual disability.Mutations in the KDM5C ARID Domain and Their Plausible Association with Syndromic Claes-Jensen-Type Disease.Complex intrachromosomal rearrangement in 1q leading to 1q32.2 microdeletion: a potential role of SRGAP2 in the gyrification of cerebral cortex.De novo mutations in neurological and psychiatric disorders: effects, diagnosis and prevention.Development of neurodevelopmental disorders: a regulatory mechanism involving bromodomain-containing proteinsMicroRNAs and intellectual disability (ID) in Down syndrome, X-linked ID, and Fragile X syndrome.Prenatal, Perinatal and Neonatal Risk Factors for Intellectual Disability: A Systemic Review and Meta-Analysis.Heterozygous deletion of the LRFN2 gene is associated with working memory deficits.Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability.Loss of function mutation in glutamic pyruvate transaminase 2 (GPT2) causes developmental encephalopathyMutations in MBOAT7, Encoding Lysophosphatidylinositol Acyltransferase I, Lead to Intellectual Disability Accompanied by Epilepsy and Autistic Features.Intellectual Disability in a Birth Cohort: Prevalence, Etiology, and Determinants at the Age of 4 Years.Epigenetic analysis of neurocognitive development at 1 year of age in a community-based pregnancy cohort.Genetics and the investigation of developmental delay/intellectual disability.Analysis of preplate splitting and early cortical development illuminates the biology of neurological disease.Identification and characterization of a missense mutation in the O-linked β-N-acetylglucosamine (O-GlcNAc) transferase gene that segregates with X-linked intellectual disability.A Consensus Network of Gene Regulatory Factors in the Human Frontal Lobe.Gene Coexpression Networks in Human Brain Developmental Transcriptomes Implicate the Association of Long Noncoding RNAs with Intellectual Disability.
P2860
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P2860
The genetic basis of non-syndromic intellectual disability: a review
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2010 nî lūn-bûn
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2010 թուականի Յուլիսին հրատարակուած գիտական յօդուած
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2010 թվականի հուլիսին հրատարակված գիտական հոդված
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2010年の論文
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2010年論文
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2010年論文
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2010年論文
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2010年論文
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2010年論文
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2010年论文
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name
The genetic basis of non-syndromic intellectual disability: a review
@ast
The genetic basis of non-syndromic intellectual disability: a review
@en
The genetic basis of non-syndromic intellectual disability: a review
@nl
type
label
The genetic basis of non-syndromic intellectual disability: a review
@ast
The genetic basis of non-syndromic intellectual disability: a review
@en
The genetic basis of non-syndromic intellectual disability: a review
@nl
prefLabel
The genetic basis of non-syndromic intellectual disability: a review
@ast
The genetic basis of non-syndromic intellectual disability: a review
@en
The genetic basis of non-syndromic intellectual disability: a review
@nl
P2093
P2860
P1476
The genetic basis of non-syndromic intellectual disability: a review
@en
P2093
John B Vincent
Liana Kaufman
Muhammad Ayub
P2860
P2888
P304
P356
10.1007/S11689-010-9055-2
P577
2010-07-29T00:00:00Z
P5875
P6179
1008972059