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ISBN 10: 1009530372 ISBN 13: 9781009530378
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ISBN 10: 1009530372 ISBN 13: 9781009530378
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ISBN 10: 1009530372 ISBN 13: 9781009530378
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Add to basketPaperback. Condition: New. SCN2A encodes a voltage-gated sodium channel (designated NaV1.2) vital for generating neuronal action potentials. Pathogenic SCN2A variants are associated with a diverse array of neurodevelopmental disorders featuring neonatal or infantile onset epilepsy, developmental delay, autism, intellectual disability and movement disorders. SCN2A is a high confidence risk gene for autism spectrum disorder and a commonly discovered cause of neonatal onset epilepsy. This remarkable clinical heterogeneity is mirrored by extensive allelic heterogeneity and complex genotype-phenotype relationships partially explained by divergent functional consequences of pathogenic variants. Emerging therapeutic strategies targeted to specific patterns of NaV1.2 dysfunction offer hope to improving the lives of individuals affected by SCN2A-related disorders. 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.
Published by 2009 Verlag Moewig, 2009
ISBN 10: 3868033106 ISBN 13: 9783868033106
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ISBN 10: 1009530372 ISBN 13: 9781009530378
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ISBN 10: 1009530372 ISBN 13: 9781009530378
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Published by Buena Vista Home Entertainement, 2003
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Language: German
Published by Ulisses Spiel & Medien, 2024
ISBN 10: 3987321784 ISBN 13: 9783987321788
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Published by Cambridge University Press, 2025
ISBN 10: 100953033X ISBN 13: 9781009530330
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Add to basketPaperback. Condition: New. SCN2A encodes a voltage-gated sodium channel (designated NaV1.2) vital for generating neuronal action potentials. Pathogenic SCN2A variants are associated with a diverse array of neurodevelopmental disorders featuring neonatal or infantile onset epilepsy, developmental delay, autism, intellectual disability and movement disorders. SCN2A is a high confidence risk gene for autism spectrum disorder and a commonly discovered cause of neonatal onset epilepsy. This remarkable clinical heterogeneity is mirrored by extensive allelic heterogeneity and complex genotype-phenotype relationships partially explained by divergent functional consequences of pathogenic variants. Emerging therapeutic strategies targeted to specific patterns of NaV1.2 dysfunction offer hope to improving the lives of individuals affected by SCN2A-related disorders. 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.
Language: English
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ISBN 10: 100953033X ISBN 13: 9781009530330
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Published by Kendall Hunt Publishing, 2021
ISBN 10: 1792453639 ISBN 13: 9781792453632
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Published by West Academic Publishing, 2021
ISBN 10: 1628102047 ISBN 13: 9781628102048
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ISBN 10: 1628102047 ISBN 13: 9781628102048
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ISBN 10: 1628102047 ISBN 13: 9781628102048
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