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Autor:
Leonardo M. Cortez, Anneliese J. Morrison, Craig R. Garen, Sawyer Patterson, Toshi Uyesugi, Rafayel Petrosyan, Rohith Vedhthaanth Sekar, Michael J. Harms, Michael T. Woodside, Valerie L. Sim
Publikováno v:
Protein Science. 31
Prion diseases are fatal neurodegenerative diseases caused by pathogenic misfolding of the prion protein, PrP. They are transmissible between hosts, and sometimes between different species, as with transmission of bovine spongiform encephalopathy to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21d0a6994bd6d8192a376200d08696fd
https://doi.org/10.1002/pro.4477
https://doi.org/10.1002/pro.4477
