Does the Clinical Phenotype of Fatal Familial Insomnia Depend on PRNP codon 129 Methionine-Valine Polymorphism?

Fatal familial insomnia (FFI) is a rare, hereditary prion-protein disease. Methionine-valine polymorphism at codon 129 of the prion-protein gene (PRNP) determines the phenotype in other hereditary prion-protein diseases, but association with the clinical phenotype in FFI remains uncertain. Early cli...

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Autori principali: Rupprecht, Sven, Grimm, Alexander, Schultze, Torsten, Zinke, Jan, Karvouniari, Panagiota, Axer, Hubertus, Witte, Otto W., Schwab, Matthias
Natura: Artigo
Lingua:Inglês
Pubblicazione: American Academy of Sleep Medicine 2013
Soggetti:
New Research
Accesso online:https://ncbi.nlm.nih.gov/pmc/articles/PMC3836347/
https://ncbi.nlm.nih.gov/pubmed/24340298
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.5664/jcsm.3286
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