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Codon 200 mutation in a new Creutzfeldt-Jakob disease family of Chilean origin

✍ Scribed by Salvatore, M.; Macchi, G.; Galvez, S.; Fieschi, C.; Petraroli, R.; Cardone, F.; Masullo, C.; Pocchiari, M.


Book ID
124109965
Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
182 KB
Volume
15
Category
Article
ISSN
0197-4580

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Creutzfeldt-Jakob disease (CJD) belongs to a group of chronic, progressive, neurodegenerative disorders that may be hereditary, infectious, or sporadic. Hereditary CJDs are associated with mutations in the PRNP gene on chromosome 20p12-pter. We report a family in which four patients developed classi