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Published by Frank Schaffer Publications, 2012
ISBN 10: 1609964799 ISBN 13: 9781609964795
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Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
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paperback. Condition: Very Good. Cover and edges may have some wear.
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Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
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Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
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Published by Cambridge University Press, GB, 2025
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.
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ISBN 10: 1009530372 ISBN 13: 9781009530378
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Language: English
Published by Cambridge University Press, 2025
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Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
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Language: English
Published by White Wolf Publishing, Inc., Clarkston, CA, 1996
ISBN 10: 156504701X ISBN 13: 9781565047013
Seller: George Strange's Bookmart, Brandon, MB, Canada
Soft cover. Condition: Near Fine. Beel, Stuart P.; Diterlizzi, Tony; Fields, Lee; Fooden, Dave; Jackson, Mark; LeBlanc, Brian; Kudelka, Andrew; McKinney, Heather; Rex, Adam; Timbrook, Joshua Gabriel; Tucker, Drew (illustrator). Bructo, Phil; Cassada, Jackie; Dansky, Richard: Hatshorn, Jennifer; Hatch, Robert; Herman, Stephan; Howard, Chris; Lemke, Ian; McCoy, Angel; Mick, Neil; Rea, Nicky PLAYERS GUIDE FOR CHANGELING: THE DREAMING Clarkston, CA: White Wolf Publishing, Inc. 1996 NF 190pp. 4to. Cover does show some shelf wear with light wear and bumping along the edges. There is a small tear at the top of the spine on the front cover. Text is clean and colours are bright. Binding has loosened inside the front cover but remains strong throughout the book. Overall book is in near fine condition and has lasted very well. *This book is oversized and may require extra shipping charges.*.
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
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Paperback. Condition: New. Brand New! Fast Delivery This is an International Edition and ship within 24-48 hours. Deliver by FedEx and Dhl, & Aramex, UPS, & USPS and we do accept APO and PO BOX Addresses. Order can be delivered worldwide within 7-12 days and we do have flat rate for up to 2LB. Extra shipping charges will be requested if the Book weight is more than 5 LB. This Item May be shipped from India, United states & United Kingdom. Depending on your location and availability.
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Add to basketPaperback. Condition: Brand New. 425 pages. 9.00x6.00x1.00 inches. In Stock.
Published by P B T Publishing House/Thomas House Publications, 1992
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First Edition
Hardcover. Condition: Used - Very Good. First Edition. Limited edition of 100 copies; Brown fabric over boards with gilt stamped text on spine and cover. Minor scuffing to covers, corners square, book block clean, square and tight.
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ISBN 10: 100953033X ISBN 13: 9781009530330
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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.
Language: English
Published by Cambridge University Press, 2025
ISBN 10: 1009530372 ISBN 13: 9781009530378
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Add to basketPaperback. Condition: Brand New. 75 pages. 6.00x0.20x9.00 inches. In Stock. This item is printed on demand.
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ISBN 10: 100953033X ISBN 13: 9781009530330
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ISBN 10: 100953033X ISBN 13: 9781009530330
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