Case report of homozygous E200D mutation of PRNP in apparently sporadic Creutzfeldt-Jakob disease. (2021)
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1186/s12883-021-02274-w
PubMed Identifier: 34182938
Publication URI: http://europepmc.org/abstract/MED/34182938
Type: Journal Article/Review
Volume: 21
Parent Publication: BMC neurology
Issue: 1
ISSN: 1471-2377