Amanote Research

Amanote Research

    RegisterSign In

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

New England Journal of Medicine - United States
doi 10.1056/nejmc1610003
Full Text
Open PDF
Abstract

Available in full text

Categories
Medicine
Date

January 19, 2017

Authors
Tzehow MokZane JaunmuktaneSusan JoinerTracy CampbellCatherine MorganBenjamin WakerleyFarhad GolestaniPeter RudgeSimon MeadH. Rolf JägerJonathan D.F. WadsworthSebastian BrandnerJohn Collinge
Publisher

Massachusetts Medical Society


Related search

Variant Creutzfeldt-Jakob Disease

English

Creutzfeldt-Jakob Disease Associated With a Missense Mutation at Codon 200 of the Prion Protein Gene in Brazil

Dementia e Neuropsychologia
GerontologyGeriatricsNeurologySensory SystemsCognitive Neuroscience
2007English

Creutzfeldt–Jakob Disease

2015English

Creutzfeldt-Jakob Disease

The Lancet
Medicine
1996English

Creutzfeldt-Jakob Disease

The Lancet
Medicine
1991English

Creutzfeldt–Jakob Disease

English

Creutzfeldt-Jakob Disease

English

Creutzfeldt-Jakob Disease

2017English

Creutzfeldt-Jakob Disease

American Journal of Medicine
Medicine
1984English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2025 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy