Atypical phenotype of 3bp deletion and burden analysis of rare variants in the exon 5 of DYT1 in primary dystonia. (October 2020)
- Record Type:
- Journal Article
- Title:
- Atypical phenotype of 3bp deletion and burden analysis of rare variants in the exon 5 of DYT1 in primary dystonia. (October 2020)
- Main Title:
- Atypical phenotype of 3bp deletion and burden analysis of rare variants in the exon 5 of DYT1 in primary dystonia
- Authors:
- Gu, X.
Chen, Y.
Yang, J.
Ou, R.
Shang, H. - Abstract:
- Is Part Of:
- Parkinsonism & related disorders. Volume 79(2020) Supplement 1
- Journal:
- Parkinsonism & related disorders
- Issue:
- Volume 79(2020) Supplement 1
- Issue Display:
- Volume 79, Issue 1 (2020)
- Year:
- 2020
- Volume:
- 79
- Issue:
- 1
- Issue Sort Value:
- 2020-0079-0001-0000
- Page Start:
- e104
- Page End:
- e105
- Publication Date:
- 2020-10
- Subjects:
- 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.2020.06.380 ↗
- 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:
- 22469.xml