SLNSW-CNTNAP2 gene dosage variation is associated with ...-TN_cdi_proquest_miscellaneous_759319434

CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

Full title: CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

Author/creator: Friedman, J, Vrijenhoek, T, Markx, S, Janssen, I.M, Vliet, W.A. van der, Faas, B.H.W, Knoers, N.V.A.M, Cahn, W, Kahn, R.S, Edelmann, L, Davis, K.L, Silverman, J.M, Brunner, H.G, Geurts van Kessel, A.H.M, Wijmenga, C, Ophoff, R.A, Veltman, J.A.

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Record Identifier: TN_cdi_proquest_miscellaneous_759319434

Language: English

Formats: Articles

Publishers: Basingstoke: Nature Publishing Group

Permalink: https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_759319434

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    CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

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    TN_cdi_proquest_miscellaneous_759319434

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    CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

    Full title

    CNTNAP2 gene dosage variation is associated with schizophrenia and epilepsy

    Author / Creator

    Friedman, J ; Vrijenhoek, T ; Markx, S ; Janssen, I.M ; Vliet, W.A. van der ; Faas, B.H.W ; Knoers, N.V.A.M ; Cahn, W ; Kahn, R.S ; Edelmann, L ; Davis, K.L ; Silverman, J.M ; Brunner, H.G ; Geurts van Kessel, A.H.M ; Wijmenga, C ; Ophoff, R.A ; Veltman, J.A

    Publisher

    Basingstoke: Nature Publishing Group

    Journal title

    Molecular psychiatry, 2008, Vol.13 (3), p.261-6

    Record Identifier

    TN_cdi_proquest_miscellaneous_759319434

    Language

    English

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    Articles

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    Adult Adult and adolescent clinical studies Biological and medical sciences Causes of Chromosomes, Human, Pair 7 CNTNAP2 gene Cognitive ability Copy number Dosage Dosage compensation (Genetics) Epilepsy Epilepsy - genetics Evaluation Female Gene dosage Gene Dosage - genetics Genetic aspects Genetic code Genetic Predisposition to Disease Genomics Haploinsufficiency Headache. Facial pains. Syncopes. Epilepsia. Intracranial hypertension. Brain oedema. Cerebral palsy Health aspects Humans In Situ Hybridization, Fluorescence - methods Intellectual disabilities Male Medical sciences Membrane Proteins - genetics Middle Aged Nerve Tissue Proteins - genetics Nervous system (semeiology, syndromes) Neurology Phenotypes Polymorphism, Single Nucleotide Psychology. Psychoanalysis. Psychiatry Psychopathology. Psychiatry Psychoses Schizophrenia Schizophrenia - genetics Sequence Analysis Variation

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    TN_cdi_proquest_miscellaneous_759319434

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_miscellaneous_759319434

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