Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease. [electronic resource]
Producer: 20000405Description: 1063-70 p. digitalISSN:- 0002-9297
- Amyloid -- genetics
- Chromosomes, Human, Pair 20 -- genetics
- Codon -- genetics
- Creutzfeldt-Jakob Syndrome -- epidemiology
- Europe -- epidemiology
- Europe, Eastern -- epidemiology
- Family Health
- Founder Effect
- Geography
- Haplotypes -- genetics
- Humans
- Japan -- epidemiology
- Jews -- genetics
- Linkage Disequilibrium -- genetics
- Mediterranean Region -- epidemiology
- Microsatellite Repeats -- genetics
- Point Mutation -- genetics
- Polymorphism, Single Nucleotide -- genetics
- Prevalence
- Prion Proteins
- Prions
- Protein Precursors -- genetics
No physical items for this record
Publication Type: Journal Article
There are no comments on this title.
Log in to your account to post a comment.