Movement Disorders (revue)

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Genetic Creutzfeldt-Jakob Disease with R208H Mutation Presenting as Progressive Supranuclear Palsy

Identifieur interne : 001113 ( Main/Exploration ); précédent : 001112; suivant : 001114

Genetic Creutzfeldt-Jakob Disease with R208H Mutation Presenting as Progressive Supranuclear Palsy

Auteurs : Radoslav Matej [République tchèque, Autriche] ; Gabor G. Kovacs [Autriche] ; Silvie Johanidesova [République tchèque] ; Ji Keller [République tchèque] ; Milada Matejckova [République tchèque] ; Jana Novakova [République tchèque] ; Vladimir Sigut [République tchèque] ; Otakar Keller [République tchèque] ; Robert Rusina [République tchèque]

Source :

RBID : Pascal:12-0183709

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Le document en format XML

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<term>Pathologie du système nerveux</term>
<term>Maladie héréditaire</term>
<term>Encéphalopathie spongiforme de Creutzfeldt-Jakob</term>
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