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Ion channel mutations underlie neuronal diseases; leaves open clinical translation and cardiovascular relevance.
ADVERTISEMENT RETURN TO ISSUEPREVReviewNEXTIon Channel Mutations in Neuronal Diseases: A Genetics PerspectiveOrtrud K. Steinlein*View Author Information Institute of Human Genetics, University Hospital, Ludwig-Maximilians-University, Goethestr. 29, D-80336 Munich, Germany*E-mail: [email protected]. Phone: (+49)89-5160-4468. Fax: (+49)89-5160-4470.Cite this: Chem. Rev. 2012, 112, 12, 6334–6352Publication Date (Web):May 18, 2012Publication History Received2 February 2012Published online18 May 2012Published inissue 12 December 2012https://pubs.acs.org/doi/10.1021/cr300044dhttps://doi.org/10.1021/cr300044dreview-articleACS PublicationsCopyright © 2012 American Chemical SocietyRequest reuse permissionsArticle Views2566Altmetric-Citations29LEARN ABOUT THESE METRICSArticle Views are the COUNTER-compliant sum of full text article downloads since November 2008 (both PDF and HTML) across all institutions and individuals. These metrics are regularly updated to reflect usage leading up to the last few days.Citations are the number of other articles citing this article, calculated by Crossref and updated daily. Find more information about Crossref citation counts.The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. Find more information on the Altmetric Attention Score and how the score is calculated. Share Add toView InAdd Full Text with ReferenceAdd Description ExportRISCitationCitation and abstractCitation and referencesMore Options Share onFacebookTwitterWechatLinked InRedditEmail Other access optionsGet e-Alertsclose SUBJECTS:Central nervous system,Diseases and disorders,Genetics,Ions,Receptors Get e-Alerts
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Ortrud K. Steinlein (2012) studied this question.
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