about
Genomic structure of the human prion protein gene.PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.Neurodegeneration in humans caused by prionsInherited prion diseases.Etiology and pathogenesis of prion diseases.Conversion of truncated and elongated prion proteins into the scrapie isoform in cultured cellsMolecular biology and pathology of scrapie and the prion diseases of humans.A novel PRNP-P105S mutation associated with atypical prion disease and a rare PrPSc conformationPrion protein transgenes and the neuropathology in prion diseases.Polymorphisms of the prion protein gene (PRNP) in a Serbian population.Identification of heterogeneous PrP gene deletions in controls by detection of allele-specific heteroduplexes (DASH)The prion diseases: Creutzfeldt-Jakob, Gerstmann-Sträussler-Scheinker, and related disorders.
P2860
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P2860
description
1990 nî lūn-bûn
@nan
1990年の論文
@ja
1990年論文
@yue
1990年論文
@zh-hant
1990年論文
@zh-hk
1990年論文
@zh-mo
1990年論文
@zh-tw
1990年论文
@wuu
1990年论文
@zh
1990年论文
@zh-cn
name
Deletion in prion protein gene in a Moroccan family
@ast
Deletion in prion protein gene in a Moroccan family
@en
type
label
Deletion in prion protein gene in a Moroccan family
@ast
Deletion in prion protein gene in a Moroccan family
@en
prefLabel
Deletion in prion protein gene in a Moroccan family
@ast
Deletion in prion protein gene in a Moroccan family
@en
P2093
P2860
P356
P1476
Deletion in prion protein gene in a Moroccan family
@en
P2093
Chatelain J
Gazengel C
Laplanche JL
P2860
P356
10.1093/NAR/18.22.6745
P407
P577
1990-11-01T00:00:00Z