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المؤلفون: D. Carleton Gajdusek, Paul Brown, Lev G. Goldfarb, Lucila Autilio-Gambetti, Pierluigi Gambeffi, Pietro Cortelli, Pasquale Montagna, Elio Lugaresi, L. Monari, Robert B. Petersen, Massimo Tabaton
المصدر: Molecular Neurobiology. 8:99-103
مصطلحات موضوعية: Prions, Mutant, Neuroscience (miscellaneous), Biology, Creutzfeldt-Jakob Syndrome, Prion Diseases, PRNP, Cellular and Molecular Neuroscience, mental disorders, Genotype, medicine, Humans, Point Mutation, Amino Acid Sequence, Gene, Fatal familial insomnia, Genetics, Polymorphism, Genetic, Genetic heterogeneity, Point mutation, Brain, medicine.disease, Virology, nervous system diseases, Phenotype, Neurology, Tomography, Emission-Computed
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9264e7ea1b7af1b33deaaa1f76ae23d9Test
https://doi.org/10.1007/bf02780659Test -
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المؤلفون: Larisa Cervenakova, Lev G. Goldfarb, Paul Brown, D. Carleton Gajdusek
المصدر: Molecular neurobiology. 8(2-3)
مصطلحات موضوعية: Male, Amyloid, Prions, Molecular Sequence Data, Neuroscience (miscellaneous), Chromosomes, Human, Pair 20, Biology, Creutzfeldt-Jakob Syndrome, Cellular and Molecular Neuroscience, Germline mutation, mental disorders, medicine, Genetic predisposition, Humans, Point Mutation, Amino Acid Sequence, Codon, Genetics, Fatal familial insomnia, Point mutation, medicine.disease, Virology, nervous system diseases, Pedigree, Phenotype, Neurology, Kuru, Female, Chromosome 20
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::48b08b433bf7e3ff57f1f8976ac07243Test
https://pubmed.ncbi.nlm.nih.gov/7999318Test