Loss-of-Function CNKSR2 Mutation Is a Likely Cause of Non-Syndromic X-Linked Intellectual Disability.
about
XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencingX-exome sequencing of 405 unresolved families identifies seven novel intellectual disability genesThe CNK2 scaffold interacts with vilse and modulates Rac cycling during spine morphogenesis in hippocampal neurons.miRNA and miRNA target genes in copy number variations occurring in individuals with intellectual disability.MECP2 Is a Frequently Amplified Oncogene with a Novel Epigenetic Mechanism That Mimics the Role of Activated RAS in MalignancyRecurrent De Novo Mutations Disturbing the GTP/GDP Binding Pocket of RAB11B Cause Intellectual Disability and a Distinctive Brain Phenotype.Genetic etiologies of the electrical status epilepticus during slow wave sleep: systematic review.Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approachesmutation causes the X-linked epilepsy-aphasia syndrome: A case report and review of literaturePorf-2 = Arhgap39 = Vilse: A Pivotal Role in Neurodevelopment, Learning and Memory
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Loss-of-Function CNKSR2 Mutation Is a Likely Cause of Non-Syndromic X-Linked Intellectual Disability.
description
2011 nî lūn-bûn
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2011年の論文
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2011年論文
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2011年論文
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2011年論文
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2011年論文
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Loss-of-Function CNKSR2 Mutati ...... inked Intellectual Disability.
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Loss-of-Function CNKSR2 Mutati ...... inked Intellectual Disability.
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type
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Loss-of-Function CNKSR2 Mutati ...... inked Intellectual Disability.
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Loss-of-Function CNKSR2 Mutati ...... inked Intellectual Disability.
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Loss-of-Function CNKSR2 Mutati ...... inked Intellectual Disability.
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Loss-of-Function CNKSR2 Mutati ...... inked Intellectual Disability.
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P2093
P2860
P1476
Loss-of-Function CNKSR2 Mutati ...... inked Intellectual Disability.
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P2093
P2860
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2011-12-20T00:00:00Z