PRKAR1B mutations are a rare cause of FUS negative neuronal intermediate filament inclusion disease

Brain. 2015 Jun;138(Pt 6):e357. doi: 10.1093/brain/awu332. Epub 2014 Nov 20.

Authors

Cyril Pottier¹, Matt Baker², Dennis W Dickson², Rosa Rademakers²

Affiliations

¹ Department of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA pottier.cyril@mayo.edu.
² Department of Neuroscience, Mayo Clinic, Jacksonville, Florida, USA.

No abstract available

Publication types

Letter
Comment

MeSH terms

Cyclic AMP-Dependent Protein Kinase RIbeta Subunit / genetics*
Female
Humans
Male
Neurodegenerative Diseases / genetics*
Neurodegenerative Diseases / pathology*
Polymorphism, Single Nucleotide / genetics*

Substances

Cyclic AMP-Dependent Protein Kinase RIbeta Subunit