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Ion channel diseases

Author: Guy Rouleau; Claudia Gaspar, Ph. D.
Publisher: Amsterdam ; Boston : Academic Press, ©2008.
Series: Advances in genetics, 63.
Edition/Format:   eBook : Document : EnglishView all editions and formats
Summary:
Ion channel dysfunction in humans leads to impairment of the excitable processes necessary for the normal function of several tissues, such as muscle and brain. It follows that an increasing number of human diseases have been associated with malfunctioning ion channels, many of which have a genetic component. This volume presents a broad and comprehensive overview of the inherited channelopathies in humans,  Read more...
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Genre/Form: Electronic books
Additional Physical Format: Print version:
Ion channel diseases.
Amsterdam ; Boston : Academic Press, ©2008
(OCoLC)234450069
Material Type: Document, Internet resource
Document Type: Internet Resource, Computer File
All Authors / Contributors: Guy Rouleau; Claudia Gaspar, Ph. D.
ISBN: 9780080923109 0080923100 9780123745279 0123745276
OCLC Number: 391052138
Language Note: Text in English.
Description: 1 online resource (x, 157 pages) : illustrations.
Contents: Periodic paralysis / Bertrand Fontaine --
Myotonia congenita / Christoph Lossin and Alfred L. George, Jr. --
Familial hemiplegic migraine / Curtis F. Barrett [and others] --
Genetics and molecular pathophysiology of Na [v below line] 1.7-related pain syndromes / Sulayman D. Dib-Hajj, Yong Yang, and Stephen G. Waxman --
Channelopathies of transepithelial transport and vesicular function / Christian A. Hübner and Thomas J. Jentsch.
Series Title: Advances in genetics, 63.
Responsibility: edited by Guy Rouleau, Claudia Gaspar.

Abstract:

Ion channel dysfunction in humans leads to impairment of the excitable processes necessary for the normal function of several tissues, such as muscle and brain. It follows that an increasing number of human diseases have been associated with malfunctioning ion channels, many of which have a genetic component. This volume presents a broad and comprehensive overview of the inherited channelopathies in humans, including clinical, genetic and molecular aspects of these conditions, as well as novel genomic and modeling research approaches. Also included is a review of potential therapeutic approac.

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