SLNSW-Variant Creutzfeldt–Jakob Disease in a Patient wi...-TN_cdi_proquest_journals_1860183798

Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

Full title: Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

Author/creator: Mok, Tzehow, Jaunmuktane, Zane, Joiner, Susan, Campbell, Tracy, Morgan, Catherine, Wakerley, Benjamin, Golestani, Farhad, Rudge, Peter, Mead, Simon, Jäger, H. Rolf, Wadsworth, Jonathan D.F, Brandner, Sebastian, Collinge, John.

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Record Identifier: TN_cdi_proquest_journals_1860183798

Language: English

Formats: Articles

Publishers: United States: Massachusetts Medical Society

Permalink: https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1860183798

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    Record title

    Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

    Record identifier

    TN_cdi_proquest_journals_1860183798

    Record permalink

    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1860183798

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    Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

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    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1860183798

    Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

    Full title

    Variant Creutzfeldt–Jakob Disease in a Patient with Heterozygosity at PRNP Codon 129

    Author / Creator

    Mok, Tzehow ; Jaunmuktane, Zane ; Joiner, Susan ; Campbell, Tracy ; Morgan, Catherine ; Wakerley, Benjamin ; Golestani, Farhad ; Rudge, Peter ; Mead, Simon ; Jäger, H. Rolf ; Wadsworth, Jonathan D.F ; Brandner, Sebastian ; Collinge, John

    Publisher

    United States: Massachusetts Medical Society

    Journal title

    The New England journal of medicine, 2017, Vol.376 (3), p.292-294

    Record Identifier

    TN_cdi_proquest_journals_1860183798

    Language

    English

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    Articles

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    Adult Brain - diagnostic imaging Brain - pathology Brain research BSE Creutzfeldt-Jakob disease Creutzfeldt-Jakob Syndrome - genetics Disease Fatal Outcome Genotype & phenotype Heterozygosity Heterozygote Humans Magnetic Resonance Imaging Male Prion protein Prion Proteins - genetics

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    TN_cdi_proquest_journals_1860183798

    Permalink

    https://collection.sl.nsw.gov.au/record/TN_cdi_proquest_journals_1860183798

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