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Diagnosis of Methionine/Valine Variant Creutzfeldt - Jakob disease using PMCA in Cerebrospinal fluid

Archive ouverte | Bougard, Daisy | CCSD

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Diagnosis of Methionine/Valine Variant Creutzfeldt - Jakob disease using PMCA in Cerebrospinal fluid.

Archive ouverte | Bougard, Daisy | CCSD

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Archive ouverte | Bougard, Daisy | CCSD

International audience. A patient with a heterozygous variant of Creutzfeldt-Jakob disease (CJD) with a methionine/valine genotype at codon 129 of the prion protein gene was recently reported. Using an ultrasensitiv...

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