Variant Creutzfeldt-jakob Disease
What's New
Last Posted: Jul 26, 2023
- Risk of variant Creutzfeldt-Jakob disease in a simulated cohort of Canadian blood donors.
Alexis Pozzo di Borgo, et al. Vox sanguinis 2023 0 - Diagnosis of Methionine/Valine Variant Creutzfeldt-Jakob Disease by Protein Misfolding Cyclic Amplification.
Bougard Daisy, et al. Emerging infectious diseases 2018 0 (7) 1364-1366 - Scrapie susceptibility-associated indel polymorphism of shadow of prion protein gene (SPRN) in Korean native black goats.
Kim Yong-Chan, et al. Scientific reports 2019 0 (1) 15261 - Variant Creutzfeldt-Jakob disease strain is identical in individuals of two PRNP codon 129 genotypes.
Brain : a journal of neurology 2019 0 (5) e22 - Human Prion Disease Surveillance in Washington State, 2006-2017.
Sánchez-González Liliana et al. JAMA network open 2020 Oct 3(10) e2020690 - Rare structural genetic variation in human prion diseases.
Lukic Ana, et al. Neurobiology of aging 2015 5 (5) 2004.e1-8 - Variant Creutzfeldt-Jakob disease
- Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP.
Mead Simon, et al. Human molecular genetics 2012 4 (8) 1897-906 - Genome-wide study links MTMR7 gene to variant Creutzfeldt-Jakob risk.
Sanchez-Juan Pascual, et al. Neurobiology of aging 2012 7 (7) 1487.e21-8 - PRNP variation in UK sporadic and variant Creutzfeldt Jakob disease highlights genetic risk factors and a novel non-synonymous polymorphism.
Bishop Matthew T, et al. BMC medical genetics 2009 12 (1) 1
More
About Rare Diseases PHGKB
Rare Disease PHGKB is an online, continuously updated, searchable database of published scientific literature, CDC and NIH resources, and other information that address the public health impact and translation of genomic and other precision health discoveries into improved health outcomes related to rare diseases...more
Content Summary
Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by the CDC Office of Public Health Genomics to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2023
- Page last updated:Sep 29, 2023
- Content source: