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	1.	TRPM1 forms ion channels associated with melanin content in melanocytes. [electronic resource] by Oancea, Elena Vriens, Joris Brauchi, Sebastian Jun, Janice Splawski, Igor Clapham, David E Producer: 20090925 In: Science signaling vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Compound mutations: a common cause of severe long-QT syndrome. [electronic resource] by Westenskow, Peter Splawski, Igor Timothy, Katherine W Keating, Mark T Sanguinetti, Michael C Producer: 20040810 In: Circulation vol. 109 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	CACNA1H mutations in autism spectrum disorders. [electronic resource] by Splawski, Igor Yoo, Dana S Stotz, Stephanie C Cherry, Allison Clapham, David E Keating, Mark T Producer: 20061016 In: The Journal of biological chemistry vol. 281 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A cardiac arrhythmia syndrome caused by loss of ankyrin-B function. [electronic resource] by Mohler, Peter J Splawski, Igor Napolitano, Carlo Bottelli, Georgia Sharpe, Leah Timothy, Katherine Priori, Silvia G Keating, Mark T Bennett, Vann Producer: 20040805 In: Proceedings of the National Academy of Sciences of the United States of America vol. 101 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Severe arrhythmia disorder caused by cardiac L-type calcium channel mutations. [electronic resource] by Splawski, Igor Timothy, Katherine W Decher, Niels Kumar, Pradeep Sachse, Frank B Beggs, Alan H Sanguinetti, Michael C Keating, Mark T Producer: 20050727 In: Proceedings of the National Academy of Sciences of the United States of America vol. 102 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Impaired interaction between the slide helix and the C-terminus of Kir2.1: a novel mechanism of Andersen syndrome. [electronic resource] by Decher, Niels Renigunta, Vijay Zuzarte, Marylou Soom, Malle Heinemann, Stefan H Timothy, Katherine W Keating, Mark T Daut, Jürgen Sanguinetti, Michael C Splawski, Igor Producer: 20071127 In: Cardiovascular research vol. 75 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Variant of SCN5A sodium channel implicated in risk of cardiac arrhythmia. [electronic resource] by Splawski, Igor Timothy, Katherine W Tateyama, Michihiro Clancy, Colleen E Malhotra, Alka Beggs, Alan H Cappuccio, Francesco P Sagnella, Giuseppe A Kass, Robert S Keating, Mark T Producer: 20020909 In: Science (New York, N.Y.) vol. 297 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	An intronic mutation causes long QT syndrome. [electronic resource] by Zhang, Li Vincent, G Michael Baralle, Marco Baralle, Francisco E Anson, Blake D Benson, D Woodrow Whiting, Bryant Timothy, Katherine W Carlquist, John January, Craig T Keating, Mark T Splawski, Igor Producer: 20041021 In: Journal of the American College of Cardiology vol. 44 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Ca(V)1.2 calcium channel dysfunction causes a multisystem disorder including arrhythmia and autism. [electronic resource] by Splawski, Igor Timothy, Katherine W Sharpe, Leah M Decher, Niels Kumar, Pradeep Bloise, Raffaella Napolitano, Carlo Schwartz, Peter J Joseph, Robert M Condouris, Karen Tager-Flusberg, Helen Priori, Silvia G Sanguinetti, Michael C Keating, Mark T Producer: 20041208 In: Cell vol. 119 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing. [electronic resource] by Ackerman, Michael J Splawski, Igor Makielski, Jonathan C Tester, David J Will, Melissa L Timothy, Katherine W Keating, Mark T Jones, Gregg Chadha, Monica Burrow, Christopher R Stephens, J Claiborne Xu, Chuanbo Judson, Richard Curran, Mark E Producer: 20050628 In: Heart rhythm vol. 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)