A novel mutation I215V in the PRNP gene associated with Creutzfeldt-Jakob and Alzheimer's diseases in three patients with divergent clinical phenotypes. [electronic resource]
Producer: 20130614Description: 77-84 p. digitalISSN:- 1432-1459
- 14-3-3 Proteins -- cerebrospinal fluid
- Aged
- Aged, 80 and over
- Alzheimer Disease -- cerebrospinal fluid
- Autopsy
- Creutzfeldt-Jakob Syndrome -- cerebrospinal fluid
- Glial Fibrillary Acidic Protein -- metabolism
- Humans
- Isoleucine -- genetics
- Male
- Models, Molecular
- Mutation -- genetics
- Phenotype
- Prion Proteins
- Prions -- genetics
- Spain
- Valine -- genetics
No physical items for this record
Publication Type: Case Reports; Journal Article; Research Support, Non-U.S. Gov't
There are no comments on this title.
Log in to your account to post a comment.