Genetics of prion diseases
Author:
Funder
Medical Research Council (MRC), UK
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference45 articles.
1. Prion diseases of humans and animals: their causes and molecular basis;Collinge;Ann Rev Neurosci,2001
2. Variant Creutzfeldt–Jakob disease: an update;Ironside;Folia Neuropathol,2012
3. Insertion in prion protein gene in familial Creutzfeldt–Jakob disease;Owen;Lancet,1989
4. Linkage of a prion protein missense variant to Gerstmann–Straussler syndrome;Hsiao;Nature,1989
5. Homozygous prion protein genotype predisposes to sporadic Creutzfeldt–Jakob disease;Palmer;Nature,1991
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1. White matter abnormalities in healthy E200K carriers may serve as an early biomarker for genetic Creutzfeldt-Jakob disease (gCJD);Journal of Neurology, Neurosurgery & Psychiatry;2024-07-30
2. Neuropathologically directed profiling of PRNP somatic and germline variants in sporadic human prion disease;Acta Neuropathologica;2024-07-24
3. Neuropathologically-directed profiling ofPRNPsomatic and germline variants in sporadic human prion disease;2024-06-29
4. Single nucleotide polymorphisms (SNPs) in the open reading frame (ORF) of prion protein gene (PRNP) in Nigerian livestock species;BMC Genomics;2024-02-14
5. Genetic diversity and breed-informative SNPs identification in domestic pig populations using coding SNPs;Frontiers in Genetics;2023-11-16
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