A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism. (April 2017)
- Record Type:
- Journal Article
- Title:
- A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism. (April 2017)
- Main Title:
- A novel de-novo mutation in the ATP1A3 gene causing rapid-onset dystonia parkinsonism
- Authors:
- Wenzel, Gregor R.
Lohmann, Katja
Kühn, Andrea A. - Abstract:
- Is Part Of:
- Parkinsonism & related disorders. Volume 37(2017)
- Journal:
- Parkinsonism & related disorders
- Issue:
- Volume 37(2017)
- Issue Display:
- Volume 37, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 37
- Issue:
- 2017
- Issue Sort Value:
- 2017-0037-2017-0000
- Page Start:
- 120
- Page End:
- 122
- Publication Date:
- 2017-04
- Subjects:
- ATP1A3 -- Haplotype-analysis -- De-novo-mutation -- RDP -- DYT12
Parkinson's disease -- Periodicals
Movement disorders -- Periodicals
Movement Disorders -- Periodicals
Nerve Degeneration -- Periodicals
Nervous System Diseases -- Periodicals
Parkinson Disease -- Periodicals
Tremor -- Periodicals
Parkinson, Maladie de -- Périodiques
Parkinson's disease
616.833 - Journal URLs:
- http://www.sciencedirect.com/science/journal/13538020 ↗
http://www.clinicalkey.com/dura/browse/journalIssue/13538020 ↗
http://www.clinicalkey.com.au/dura/browse/journalIssue/13538020 ↗
http://www.prd-journal.com/ ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.parkreldis.2017.02.009 ↗
- Languages:
- English
- ISSNs:
- 1353-8020
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6406.787000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 1146.xml