Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability

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• Excess of De Novo Deleterious Mutations in Genes Associated with Glutamatergic Systems in Nonsyndromic Intellectual Disability
  per: Hamdan, Fadi F., et al.
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• Mutations in SYNGAP1 in Autosomal Nonsyndromic Mental Retardation
  per: Hamdan, Fadi F., et al.
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• De Novo Mutations in FOXP1 in Cases with Intellectual Disability, Autism, and Language Impairment
  per: Hamdan, Fadi F., et al.
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• Dinucleotide repeat polymorphism at the human CRYB2 gene locus (22q11.2)
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