Format

Send to

Choose Destination
Brain. 2019 Mar 7. pii: awz041. doi: 10.1093/brain/awz041. [Epub ahead of print]

Biallelic POLR3A variants confirmed as a frequent cause of hereditary ataxia and spastic paraparesis.

Author information

1
Institute of Clinical Medicine, University of Oslo, Norway.
2
Department of Neurology, Oslo University Hospital, Norway.
3
Department of Neurology, Vestre Viken Hospital, Norway.
4
Department of Medical Genetics, Oslo University Hospital, Norway.
5
Department of Radiology and Nuclear Medicine, Oslo University Hospital, Norway.
6
Department of Ophthalmology, Oslo University Hospital, Norway.
7
Department of Clinical Neurophysiology, Oslo University Hospital, Norway.
8
Department of Medical Biochemistry, University of Oslo, Norway.
9
Department of Microbiology, Oslo University Hospital, Norway.
10
Department of Research and Development, Division of Neuroscience, Oslo University Hospital and the University of Oslo, Norway.
11
National Centre for Epilepsy, Oslo University Hospital, Norway.
PMID:
30847471
DOI:
10.1093/brain/awz041

Supplemental Content

Full text links

Icon for Silverchair Information Systems Icon for Norwegian BIBSYS system
Loading ...
Support Center