Familial Creutzfeldt-Jakob disease with an R208H-129V haplotype and Kuru plaques. [electronic resource]
Producer: 20060425Description: 449-52 p. digitalISSN:- 0003-9942
- Amyloid -- genetics
- Arginine -- genetics
- Blotting, Western -- methods
- Brain -- pathology
- Creutzfeldt-Jakob Syndrome -- genetics
- Haplotypes
- Histidine -- genetics
- Humans
- Immunohistochemistry -- methods
- Male
- Middle Aged
- Mutation
- Plaque, Amyloid -- pathology
- Prion Proteins
- Prions
- Protein Precursors -- genetics
- Valine -- genetics
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Publication Type: Case Reports; Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
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