De novo KCNA2 mutations cause hereditary spastic paraplegia. Issue 2 (23rd February 2017)
- Record Type:
- Journal Article
- Title:
- De novo KCNA2 mutations cause hereditary spastic paraplegia. Issue 2 (23rd February 2017)
- Main Title:
- De novo KCNA2 mutations cause hereditary spastic paraplegia
- Authors:
- Manole, Andreea
Männikkö, Roope
Hanna, Michael G.
Kullmann, Dimitri M.
Houlden, Henry - Abstract:
- Is Part Of:
- Annals of neurology. Volume 81:Issue 2(2017)
- Journal:
- Annals of neurology
- Issue:
- Volume 81:Issue 2(2017)
- Issue Display:
- Volume 81, Issue 2 (2017)
- Year:
- 2017
- Volume:
- 81
- Issue:
- 2
- Issue Sort Value:
- 2017-0081-0002-0000
- Page Start:
- 326
- Page End:
- 328
- Publication Date:
- 2017-02-23
- Subjects:
- Neurology -- Periodicals
Pediatric neurology -- Periodicals
Nervous system -- Surgery -- Periodicals
616.8 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1531-8249 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/109668537 ↗
http://www3.interscience.wiley.com/cgi-bin/jhome/76507645 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/ana.24866 ↗
- Languages:
- English
- ISSNs:
- 0364-5134
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1043.140000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5572.xml