Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene

scientific article published in April 2003

Phenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1046/J.1365-2990.2003.00423.X
P8608Fatcat IDrelease_fgjfabq5drfadapyxof5fo7d54
P698PubMed publication ID12662318

P50authorPéter LantosQ1127948
P2093author name stringRossor M
King A
Collinge J
Doey L
Mead S
P2860cites workAn inherited prion disease with a PrP P105L mutation: clinicopathologic and PrP heterogeneityQ33688704
Fatal familial insomnia: clinical and pathologic heterogeneity in genetic half brothersQ48327510
Familial prion disease with a novel 144-bp insertion in the prion protein gene in a Basque family.Q48672320
P433issue2
P921main subjectprion protein familyQ24724413
P304page(s)98-105
P577publication date2003-04-01
P1433published inNeuropathology and Applied NeurobiologyQ7002494
P1476titlePhenotypic variability in the brains of a family with a prion disease characterized by a 144-base pair insertion in the prion protein gene
P478volume29

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cites work (P2860)
Q35103451A case of Gerstmann-Sträussler-Scheinker disease with a novel six octapeptide repeat insertion
Q33966829Analysis of the [RNQ+] prion reveals stability of amyloid fibers as the key determinant of yeast prion variant propagation
Q49076261Biology and neuropathology of prion diseases
Q38924501Cerebellar compartmentation of prion pathogenesis
Q28910222Early onset prion disease from octarepeat expansion correlates with copper binding properties
Q36226900Familial prion disease in a Hungarian family with a novel 144-base pair insertion in the prion protein gene
Q33716193Filamentous white matter prion protein deposition is a distinctive feature of multiple inherited prion diseases
Q47577189Gerstmann-Sträussler-Scheinker disease with atypical presentation.
Q37355539Insights into intragenic and extragenic effectors of prion propagation using chimeric prion proteins
Q36310865Phenotypic variability in human prion diseases.
Q36359872Prion disease genetics
Q33325657Prion protein insertional mutations increase aggregation propensity but not fiber stability
Q35950108Prion protein repeat expansion results in increased aggregation and reveals phenotypic variability.
Q36774861Protease-sensitive prions with 144-bp insertion mutations

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