Cargando…
Association of a null allele of SPRN with variant Creutzfeldt–Jakob disease
BACKGROUND: No susceptibility genes have been identified in human prion disase, apart from the prion protein gene (PRNP). The gene SPRN, encodes Shadoo (Sho, shadow of prion protein) which has protein homology and possible functional links with the prion protein. METHODS: A genetic screen was carrie...
Autores principales: | Beck, J A, Campbell, T A, Adamson, G, Poulter, M, Uphill, J B, Molou, E, Collinge, J, Mead, S |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2008
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2590874/ https://www.ncbi.nlm.nih.gov/pubmed/18805828 http://dx.doi.org/10.1136/jmg.2008.061804 |
Ejemplares similares
-
Genetic risk factors for variant Creutzfeldt–Jakob disease: a genome-wide association study
por: Mead, Simon, et al.
Publicado: (2009) -
Variants of PLCXD3 are not associated with variant or sporadic Creutzfeldt-Jakob disease in a large international study
por: Balendra, Rubika, et al.
Publicado: (2016) -
Familial Creutzfeldt-Jakob Disease in an Indian Kindred
por: Katrak, Sarosh M., et al.
Publicado: (2019) -
Neuronal antibodies in patients with suspected or confirmed sporadic Creutzfeldt-Jakob disease
por: Rossi, Meghan, et al.
Publicado: (2015) -
MRI findings are often missed in the diagnosis of Creutzfeldt-Jakob disease
por: Carswell, Christopher, et al.
Publicado: (2012)