𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Creutzfeldt–Jakob disease and inclusion body myositis: Abundant disease-associated prion protein in muscle

✍ Scribed by Gabor G. Kovacs; Elisabeth Lindeck-Pozza; Leila Chimelli; Abelardo Q. C. Araújo; Alberto A. Gabbai; Thomas Ströbel; Markus Glatzel; Adriano Aguzzi; Herbert Budka


Publisher
John Wiley and Sons
Year
2003
Tongue
English
Weight
333 KB
Volume
55
Category
Article
ISSN
0364-5134

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Identification of three novel mutations
✍ Katell Peoc'h; Philippe Manivet; Patrice Beaudry; Françoise Attane; Gérard Besso 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 49 KB 👁 1 views

Inherited prion diseases are characterized by mutations in the PRNP gene encoding the prion protein (PrP). As the other sporadic or infectious prion disease forms, they are almost all characterized by the accumulation in the brain of an abnormal misfolded form of the patient's PrP. Brain extracts ca