CSTB null mutation associated with microcephaly, early developmental delay, and severe dyskinesia. (1st March 2016)
- Record Type:
- Journal Article
- Title:
- CSTB null mutation associated with microcephaly, early developmental delay, and severe dyskinesia. (1st March 2016)
- Main Title:
- CSTB null mutation associated with microcephaly, early developmental delay, and severe dyskinesia
- Authors:
- Mancini, Grazia M.S.
Schot, Rachel
de Wit, Marie Claire Y.
de Coo, René F.
Oostenbrink, Rianne
Bindels-de Heus, Karen
Berger, Lieke P.V.
Lequin, Maarten H.
de Vries, Femke A.T.
Wilke, Martina
van Slegtenhorst, Marjon A. - Abstract:
- Is Part Of:
- Neurology. Volume 86:Number 9(2016)
- Journal:
- Neurology
- Issue:
- Volume 86:Number 9(2016)
- Issue Display:
- Volume 86, Issue 9 (2016)
- Year:
- 2016
- Volume:
- 86
- Issue:
- 9
- Issue Sort Value:
- 2016-0086-0009-0000
- Page Start:
- Page End:
- Publication Date:
- 2016-03-01
- Subjects:
- Neurology -- Periodicals
Neurology -- Periodicals
Neurologie -- Périodiques
616.8 - Journal URLs:
- http://www.mdconsult.com/public/search?search_type=journal&j_sort=pub_date&j_issn=0028-3878 ↗
http://www.mdconsult.com/about/journallist/192093418-5/about0nz0.html ↗
http://www.neurology.org ↗
http://journals.lww.com ↗ - DOI:
- 10.1212/WNL.0000000000002422 ↗
- Languages:
- English
- ISSNs:
- 0028-3878
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.500000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 5089.xml