De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient. (July 2019)
- Record Type:
- Journal Article
- Title:
- De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient. (July 2019)
- Main Title:
- De-novo KMT2B mutation in a consanguineous family: 15-Year follow-up of an Afghan dystonia patient
- Authors:
- Klein, Christine
Baumann, Hauke
Olschewski, Luisa
Hanssen, Henrike
Münchau, Alexander
Ferbert, Andreas
Brüggemann, Norbert
Lohmann, Katja - Abstract:
- Is Part Of:
- Parkinsonism & related disorders. Volume 64(2019)
- Journal:
- Parkinsonism & related disorders
- Issue:
- Volume 64(2019)
- Issue Display:
- Volume 64, Issue 2019 (2019)
- Year:
- 2019
- Volume:
- 64
- Issue:
- 2019
- Issue Sort Value:
- 2019-0064-2019-0000
- Page Start:
- 337
- Page End:
- 339
- Publication Date:
- 2019-07
- Subjects:
- Generalized dystonia -- Consanguinity -- KMT2B -- De-novo mutation -- Gene expression -- Dyscalculia
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.2019.03.018 ↗
- 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:
- 11657.xml