FV 20 Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development. Issue 8 (August 2019)

Record Type:: Journal Article
Title:: FV 20 Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development. Issue 8 (August 2019)
Main Title:: FV 20 Dominant SCN2A mutation causes familial episodic ataxia and impairment of speech development
Authors:: Fazeli, W.
Abstract:
Is Part Of:: Clinical neurophysiology. Volume 130:Issue 8(2019:Aug.)
Journal:: Clinical neurophysiology
Issue:: Volume 130:Issue 8(2019:Aug.)
Issue Display:: Volume 130, Issue 8 (2019)
Year:: 2019
Volume:: 130
Issue:: 8
Issue Sort Value:: 2019-0130-0008-0000
Page Start:: e131
Page End:: e132
Publication Date:: 2019-08
Subjects:: Neurophysiology -- Periodicals
Electroencephalography -- Periodicals
Electromyography -- Periodicals
Neurology -- Periodicals
612.8
Journal URLs:: http://www.sciencedirect.com/science/journal/13882457 ↗
http://www.elsevier.com/journals ↗
DOI:: 10.1016/j.clinph.2019.04.630 ↗
Languages:: English
ISSNs:: 1388-2457
Deposit Type:: Legaldeposit
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗
Physical Locations:: British Library DSC - 3286.310645
British Library DSC - BLDSS-3PM
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Ingest File:: 11008.xml