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
✦ LIBER ✦
Striking PrPsc heterogeneity in inherited prion diseases with the D178N mutation
✍ Scribed by Stéphane Haïk; Katell Peoc'h; Jean-Philippe Brandel; Nicolas Privat; Jean-Louis Laplanche; Baptiste A. Faucheux; Jean-Jacques Hauw
- Publisher
- John Wiley and Sons
- Year
- 2004
- Tongue
- English
- Weight
- 135 KB
- Volume
- 56
- Category
- Article
- ISSN
- 0364-5134
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The book is well printed and the illustrations are very adequate, most of the drawings having been copied from articles in the paediatric surgical literature. This is by far the best book on a paediatric surgical subject which has been written in East Germany and it may be hoped that it will greatly