Familial Creutzfeldt-Jakob disease associated with a point mutation at codon 210 of the prion protein gene
Document title: Familial Creutzfeldt-Jakob disease associated with a point mutation at codon 210 of the prion protein gene
Journal: Arquivos de neuro-psiquiatria
Database: PERIÓDICA
System number: 000191039
ISSN: 0004-282X
Authors: 1
Institutions: 1Universidade de Sao Paulo, Faculdade de Medicina, Sao Paulo. Brasil
Year:
Season: Dic
Volumen: 59
Number: 4
Pages: 932-935
Country: Brasil
Language: Inglés
Document type: Artículo
Approach: Aplicado, descriptivo
Disciplines: Medicina,
Química
Keyword: Neurología,
Bioquímica,
Genética,
Enfermedad de Creutzfeldt-Jakob,
Mutaciones génicas,
Priones,
Mutación puntual
Keyword: Medicine,
Chemistry,
Neurology,
Biochemistry,
Creutzfeldt-Jakob disease,
Gene mutations,
Prions,
Point mutation,
Genetics
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