Deletion in prion protein gene in a Moroccan family

Deletion in prion protein gene in a Moroccan family

Item
http://www.wikidata.org/entity/Q35890239
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

Deletion in prion protein gene in a Moroccan family

Item
http://www.wikidata.org/entity/Q35890239
description
1990 nî lūn-bûn
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1990年の論文
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1990年論文
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1990年論文
@zh-hant
1990年論文
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1990年論文
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1990年論文
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1990年论文
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1990年论文
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1990年论文
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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
P1433
P1476
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P921
P932
P356
P1433
P1476
Deletion in prion protein gene in a Moroccan family
@en
P2093
P2860
P304
P31
P356
P407
P433
P478
P577
P5875
P698
P921
P932