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Autor:
Yacov Balash, Esther Kahana, Amos D. Korczyn, Meir Wolker, Hadeel Nabal, Emilia Anis, Hanna Rosenmann, Ron Milo
Publikováno v:
Neuroepidemiology.
BACKGROUND: Sporadic Creutzfeldt-Jakob disease (s-CJD) is a rare, fatal neurodegenerative disorder. Familial cases of Creutzfeldt-Jakob disease (f-CJD) due to mutations in the PRNP gene are even rarer around the world; however, in Israel there is a f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::10f95d49ea85ea9de6f0e8a799a98d21
https://doi.org/10.1159/000530407
https://doi.org/10.1159/000530407
