SCN2A-Related Disorders

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http://doi.org/10.1017/9781009530361
Author(s)
Abbott, Megan
Bender, Kevin J.
Brunklaus, Andreas
Demarest, Scott
Egan, Shawn
Haviland, Isabel
Kearney, Jennifer A.
Schust Myers, Leah
Olson, Heather E.
Sanders, Stephan J.
SanInocencio, Christina
Symonds, Joseph
Thompson, Christopher H.
Contributor(s)
Alfred L. George, Jr. (editor)
Language
English
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Abstract
This Element provides a review of the clinical features, genetic basis, pathophysiology, pharmacology and treatment of these genetic conditions authored by leading experts in the field and accompanied by perspectives shared by affected families. This title is also available as Open Access on Cambridge Core.
URI
https://directory.doabooks.org/handle/20.500.12854/156880
Keywords
neurology and clinical neuroscience
DOI
10.1017/9781009530361
ISBN
9781009530361, 9781009530330, 9781009530378, 9781009530361
Publisher
Cambridge University Press
Publication date and place
2024
Imprint
Medicine
Series
Elements in Genetics in Epilepsy, EGE
Classification
Neurology and clinical neurophysiology
Pages
96
Rights
https://creativecommons.org/licenses/by-nc/4.0/
https://creativecommons.org/licenses/by-nc/4.0/
Except where otherwise noted, this item's license is described as https://creativecommons.org/licenses/by-nc/4.0/