Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.

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rSNPBase 3.0: an updated database of SNP-related regulatory elements, element-gene pairs and SNP-based gene regulatory networks.Genome-wide investigation of an ID cohort reveals de novo 3'UTR variants affecting gene expression

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Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.

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Next-gen sequencing identifies ...... tes in neurological disorders.

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Next-gen sequencing identifies ...... tes in neurological disorders.

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Next-gen sequencing identifies ...... tes in neurological disorders.

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Next-gen sequencing identifies ...... tes in neurological disorders.

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D F Newbury

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D Gajewski

http://www.w3.org/2001/XMLSchema#string

J Ho

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S C Vernes

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S D Smith

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X S Chen

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An integrated map of genetic variation from 1,092 human genomes

Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation

dbSNP: the NCBI database of genetic variation

UTRdb and UTRsite (RELEASE 2010): a collection of sequences and regulatory motifs of the untranslated regions of eukaryotic mRNAs

The developmental transcriptome of the human brain: implications for neurodevelopmental disorders

Analysis of protein-coding genetic variation in 60,706 humans

Impacts of variation in the human genome on gene regulation

Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets

The contribution of de novo coding mutations to autism spectrum disorder

Patterns and rates of exonic de novo mutations in autism spectrum disorders

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mp.2017.30

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scholarly article

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10.1038/MP.2017.30

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English

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2017-03-14T00:00:00Z

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5474318

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Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.

about

P2860

P2860

Next-gen sequencing identifies non-coding variation disrupting miRNA-binding sites in neurological disorders.

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