Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation. Issue 1 (26th April 2016)
- Record Type:
- Journal Article
- Title:
- Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation. Issue 1 (26th April 2016)
- Main Title:
- Exome Sequencing Identifies a Novel Homozygous Missense ATP13A2 Mutation
- Authors:
- Abbas, Masoom M.
Govindappa, Shyla T.
Sheerin, Una‐Marie
Bhatia, Kailash P.
Muthane, Uday B. - Abstract:
- Abstract : View Supplementary Video 1
- Is Part Of:
- Movement disorders clinical practice. Volume 4:Issue 1(2017)
- Journal:
- Movement disorders clinical practice
- Issue:
- Volume 4:Issue 1(2017)
- Issue Display:
- Volume 4, Issue 1 (2017)
- Year:
- 2017
- Volume:
- 4
- Issue:
- 1
- Issue Sort Value:
- 2017-0004-0001-0000
- Page Start:
- 132
- Page End:
- 135
- Publication Date:
- 2016-04-26
- Subjects:
- Kufor‐Rakeb syndrome -- exome sequence -- early onset atypical parkinsonism
Movement Disorders
Movement disorders -- Periodicals
Movement disorders
Periodicals
Periodicals
616 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/%28ISSN%292330-1619 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/mdc3.12353 ↗
- Languages:
- English
- ISSNs:
- 2330-1619
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5980.317300
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 11319.xml