Evidence for synergistic effects of PRNP and ATP7B mutations in severe neuropsychiatric deterioration

BACKGROUND: Wilson’s disease (WD), a rare cause of neuropsychiatric deterioration, is associated with mutations in the ATP7B gene. Prion diseases are also rare causes of neuropsychiatric deterioration that can occur sporadically without an identifiable cause, or can be attributed to mutations in the...

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Detalles Bibliográficos
Autores principales: Forbes, Nauzer, Goodwin, Susan, Woodward, Kevin, Morgan, David G, Brady, Lauren, Coulthart, Michael B, Tarnopolsky, Mark A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996179/
https://www.ncbi.nlm.nih.gov/pubmed/24555712
http://dx.doi.org/10.1186/1471-2350-15-22

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3996179/
https://www.ncbi.nlm.nih.gov/pubmed/24555712
http://dx.doi.org/10.1186/1471-2350-15-22

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