Загрузка...
MR Imaging of Familial Creutzfeldt-Jakob Disease: A Blinded and Controlled Study
BACKGROUND AND PURPOSE: The E200K mutation of the PRNP (prion protein) gene is the most common cause of familial Creutzfeldt-Jakob disease (fCJD), which has imaging and clinical features that are similar to the sporadic form. The purpose of this study was to conduct a controlled and blinded evaluati...
Сохранить в:
| Опубликовано в: : | AJNR Am J Neuroradiol |
|---|---|
| Главные авторы: | , , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
American Society of Neuroradiology
2008
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC8118770/ https://ncbi.nlm.nih.gov/pubmed/18635614 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3174/ajnr.A1217 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|