Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
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Strong Amerind/white sex bias and a possible Sephardic contribution among the founders of a population in northwest ColombiaA Comparison of Classical and H-Type Bovine Spongiform Encephalopathy Associated with E211K Prion Protein Polymorphism in Wild-Type and EK211 Cattle Following Intracranial Inoculation.Fatal prion disease in a mouse model of genetic E200K Creutzfeldt-Jakob diseaseMolecular, biochemical and genetic characteristics of BSE in CanadaRandom mutagenesis-PCR to introduce alterations into defined DNA sequences for validation of SNP and mutation detection methods.The expanding universe of prion diseases.Prevalence of the prion protein gene E211K variant in U.S. cattle.Creutzfeldt-Jakob disease surveillance in Argentina, 1997-2008.Snord 3A: a molecular marker and modulator of prion disease progressionAn overview of transmissible spongiform encephalopathies.Quantifying prion disease penetrance using large population control cohortsPrP(ST), a soluble, protease resistant and truncated PrP form features in the pathogenesis of a genetic prion disease.Small-molecule theranostic probes: a promising future in neurodegenerative diseases.Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation casesSpatial clusters of Creutzfeldt-Jakob disease mortality in Japan between 1995 and 2004.Codistribution of amyloid beta plaques and spongiform degeneration in familial Creutzfeldt-Jakob disease with the E200K-129M haplotype.Genetic prion disease: Experience of a rapidly progressive dementia center in the United States and a review of the literature.Clinical findings and diagnosis in genetic prion diseases in Germany.Clinical aspects of common genetic Creutzfeldt-Jakob disease.Age and origin of the PRNP E200K mutation causing familial Creutzfeldt-Jacob disease in Libyan JewsCreutzfeldt-Jakob disease associated with a missense mutation at codon 200 of the prion protein gene in Brazil.Mutation rate in human microsatellites.Gerstmann-Sträussler-Scheinker syndrome with variable phenotype in a new kindred with PRNP-P102L mutation.Deep Learning Representation from Electroencephalography of Early-Stage Creutzfeldt-Jakob Disease and Features for Differentiation from Rapidly Progressive Dementia.Haplotype analysis of a BRCA1 : 185delAG mutation in a Chilean family supports its Ashkenazi origins
P2860
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P2860
Ancestral origins and worldwide distribution of the PRNP 200K mutation causing familial Creutzfeldt-Jakob disease.
description
1999 nî lūn-bûn
@nan
1999 թուականի Ապրիլին հրատարակուած գիտական յօդուած
@hyw
1999 թվականի ապրիլին հրատարակված գիտական հոդված
@hy
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
name
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@ast
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@en
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@nl
type
label
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@ast
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@en
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@nl
prefLabel
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@ast
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@en
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@nl
P2093
P2860
P50
P356
P1476
Ancestral origins and worldwid ...... ial Creutzfeldt-Jakob disease.
@en
P2093
D C Gajdusek
H Furukawa
L Cervenakova
L G Goldfarb
N Sambuughin
P2860
P304
P356
10.1086/302340
P407
P577
1999-04-01T00:00:00Z