date: 2016-01-07T12:48:52Z
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pdf:docinfo:title: Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family
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subject: Disease gene discovery in neurodevelopmental disorders, including X-linked intellectual disability (XLID) has recently been accelerated by next-generation DNA sequencing approaches.
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dc:title: Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family
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cp:subject: Disease gene discovery in neurodevelopmental disorders, including X-linked intellectual disability (XLID) has recently been accelerated by next-generation DNA sequencing approaches.
pdf:docinfo:subject: Disease gene discovery in neurodevelopmental disorders, including X-linked intellectual disability (XLID) has recently been accelerated by next-generation DNA sequencing approaches.
pdf:docinfo:creator: Vera M. Kalscheuer and Robert J. Harvey
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dc:description: Disease gene discovery in neurodevelopmental disorders, including X-linked intellectual disability (XLID) has recently been accelerated by next-generation DNA sequencing approaches.
Keywords: ArfGEF, BRAG1, IQ-ArfGEF, IQSEC2, MRX78, XLID
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dc:creator: Vera M. Kalscheuer and Robert J. Harvey
description: Disease gene discovery in neurodevelopmental disorders, including X-linked intellectual disability (XLID) has recently been accelerated by next-generation DNA sequencing approaches.
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Last-Modified: 2016-01-07T12:48:52Z
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title: Novel Missense Mutation A789V in IQSEC2 Underlies X-Linked Intellectual Disability in the MRX78 Family
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creator: Vera M. Kalscheuer and Robert J. Harvey
dc:subject: ArfGEF, BRAG1, IQ-ArfGEF, IQSEC2, MRX78, XLID
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