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15篇 您的检索式：作者名="LE SCOUARNEC S"

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		题名	作者	年代	出处	被引量
	1	Sodium channel betal subunit mutations associated with Brugada syndrome and cardi- ac conduction disease in humans显示文摘	WatanabeH Koopmann TT le Scouarnec S	2008	JCI2008，118，：	1
	2	Sodium channel betal subunit mutations associated with Brugada syndrome and cardiac conduction disease in Humans 显示文摘	Watanabe H Koopmann TT Le Scouarnec S	2008	J Clin Invest2008，118，6：	1
	3	Sodium channel betal subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 显示文摘	Watanabe H Koopmann T T Le Scouarnec S	2008	J Clin Invest2008，118，6：	1
	4	Sodi- um channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 显示文摘	Watanabe H Koopmann TT Le Scouarnec S	2008	J Clin Invest2008，118，6：	1
	5	Defining the cellular phenotype of 'ankyrin-B syndrome' variants:human ANK2 variants associated with clinical phenotypes display a spectrum of activities in cardiomyocytes显示文摘	Mohler PJ le Scouarnec S Denjoy I	2007	Circulation2007，115，4：	1
	6	Sodium channel beta 1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 显示文摘	WATANABE H KOOPMANN T T LE SCOUARNEC S	2008	J Clin Invest2008，118，6：	1
	7	Sodium channel (31 subunit mutations associated withBrugada syndrome and cardiac conduction disease in humans显示文摘	WATANABE H KOOPMANN T T LE SCOUARNEC S etal	2008	JClin Invest2008，118，6：	1
	8	Identification of large families in early repolarization syndrome显示文摘	Gourraud JB Le Scouarnec S Sacher F		0，，02：	1
	9	Identification of large families in early repolarization syndrome显示文摘	GourraudJB Le Scouarnec S Sacher F	2013	J Am Coll Cardiol2013，61，2：	1
	10	Familial aggregation of calcific aortic valve stenosis in the western part of France显示文摘	Probst V Le Scouarnec S Legendre A		0，，06：	1
	11	Testing the burden of rare variation in arrhythmia-susceptibility genes provides new insights into molecular diagnosis for Brugada syndrome显示文摘	Le Scouarnec S Karakachoff M Gourraud JB	2015	Hum Mol Genet2015，24，10：	1
	12	Sodium channel betal subunit mutations associated with Brugada syndrome and car- ~liac conduction disease in humans显示文摘	Watanabe H Koopmann 'IT Le Scouarnec S	2008	J Clin Invest2008，118，6：	1
	13	Sodium channel betal subunit mutations associated with brugada syndrome and cardiac conduction disease in humans 显示文摘	Watanabe H Koopmann TT Le Scouarnec S	2008	Clin Invest2008，118，6：	1
	14	Sodium channel betal subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans 显示文摘	Watanabe H Koopmann TT Le Scouarnec S	2008	J Clin Invest2008，118，6：	1
	15	Regenerating codes: A system perspective 显示文摘	Jiekak S Kermarrec A M Le Scouarnec N	2013	ACM SlGOPS Operating Systems Review2013，47，2：	1

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