Article

Comparative Analysis of The Characteristics of The Chinese gCJD Patients With E196A and E196K Mutation in PRNP

2021-04-05

Abstract excerpt

<title>Abstract</title> <p><bold>Background</bold>: Genetic human prion diseases are a group of inherited encephalopathies caused by the different mutations in PrP-encoding gene <italic>PRNP. </italic>The clinical, neuropathological and laboratory features may differ largely according to the mutants at the different positions and with different amino acid. Here, we comparatively analyzed the features of 16 Chines...

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Literature Corpus work: 4beeef3e-d24b-50cf-8b25-5c700ad6a952
DOI: 10.21203/rs.3.rs-375212/v1

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