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Advances in genetics [electronic resource] . Volume 63, Ion channel diseases / edited by Guy Rouleau, Claudia Gaspar.

Contributor(s): Rouleau, Guy | Gaspar, Claudia, Ph. DMaterial type: TextTextSeries: Advances in genetics ; v. 63Publication details: Amsterdam ; Boston : Academic Press, c2008. Description: 1 online resource (x, 157 p.) : illISBN: 9780123745279 (electronic bk.); 0123745276 (electronic bk.)Other title: Ion channel diseasesSubject(s): Ion channels | Membrane disorders | Ion channels | Membrane disordersGenre/Form: Electronic books.DDC classification: 571.6/4 LOC classification: QH431.A1 | A363 2008ebOnline resources: ScienceDirect 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, 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 approaches for each of these conditions.
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Includes bibliographical references and index.

Description based on print version record.

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 approaches for each of these conditions.

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