Creutzfeldt-Jakob disease with the V203I mutation and M129V polymorphism of the prion protein gene (PRNP) and a 17 kDa prion protein fragment

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Veröffentlicht in:	Neuropathology and applied neurobiology 2010-10, Vol.36 (6), p.558-563
Hauptverfasser:	Jeong, B-H., Jeon, Y-C., Lee, Y-J., Cho, H-J., Park, S-J., Chung, D-I., Kim, J., Kim, S. H., Kim, H-T., Choi, E-K., Choi, K-C., Carp, R. I., Kim, Y-S.
Format:	Artikel
Sprache:	eng
Schlagworte:	Aged Base Sequence Biological and medical sciences Blotting, Western Brain - metabolism Brain - pathology Creutzfeldt-Jakob Syndrome - genetics Creutzfeldt-Jakob Syndrome - pathology Creutzfeldt-Jakob Syndrome - physiopathology Degenerative and inherited degenerative diseases of the nervous system. Leukodystrophies. Prion diseases Fatal Outcome Female Humans Medical sciences Molecular Sequence Data Mutation Neurology Polymerase Chain Reaction Polymorphism, Single Nucleotide Prion Proteins Prions - genetics PrPSc Proteins - genetics PrPSc Proteins - metabolism
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