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Lien Lam

Showing results (11-20 of 20) with videos related to

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Circulation|March 26, 2008
Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathyTatiana Tsoutsman, Matthew Kelly, Dominic C H Ng, et al.
Heart Rhythm|May 10, 2016
A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardiaBelinda Gray, Richard D Bagnall, Lien Lam, et al.
Journal of Molecular and Cellular Cardiology|September 5, 2006
Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathyTatiana Tsoutsman, Jessica Chung, Alessandra Doolan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2017
Identification of pathogenic gene mutations in <i>LMNA</i> and <i>MYBPC3</i> that alter RNA splicingKaoru Ito, Parth N Patel, Joshua M Gorham, et al.
Annals of Neurology|December 26, 2015
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsyRichard D Bagnall, Douglas E Crompton, Slavé Petrovski, et al.
Circulation. Genomic and Precision Medicine|August 31, 2021
Contribution of Noncanonical Splice Variants to <i>TTN</i> Truncating Variant CardiomyopathyParth N Patel, Kaoru Ito, Jon A L Willcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
The New England Journal of Medicine|June 23, 2016
A Prospective Study of Sudden Cardiac Death among Children and Young AdultsRichard D Bagnall, Robert G Weintraub, Jodie Ingles, et al.
The New England Journal of Medicine|February 17, 2012
Truncations of titin causing dilated cardiomyopathyDaniel S Herman, Lien Lam, Matthew R G Taylor, et al.
Circulation. Genomic and Precision Medicine|December 29, 2022
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (<i>DSP</i>) Truncating VariantEdgar T Hoorntje, Charlotte Burns, Luisa Marsili, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Circulation|March 26, 2008
Severe heart failure and early mortality in a double-mutation mouse model of familial hypertrophic cardiomyopathyTatiana Tsoutsman, Matthew Kelly, Dominic C H Ng, et al.
Heart Rhythm|May 10, 2016
A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardiaBelinda Gray, Richard D Bagnall, Lien Lam, et al.
Journal of Molecular and Cellular Cardiology|September 5, 2006
Molecular insights from a novel cardiac troponin I mouse model of familial hypertrophic cardiomyopathyTatiana Tsoutsman, Jessica Chung, Alessandra Doolan, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 7, 2017
Identification of pathogenic gene mutations in <i>LMNA</i> and <i>MYBPC3</i> that alter RNA splicingKaoru Ito, Parth N Patel, Joshua M Gorham, et al.
Annals of Neurology|December 26, 2015
Exome-based analysis of cardiac arrhythmia, respiratory control, and epilepsy genes in sudden unexpected death in epilepsyRichard D Bagnall, Douglas E Crompton, Slavé Petrovski, et al.
Circulation. Genomic and Precision Medicine|August 31, 2021
Contribution of Noncanonical Splice Variants to <i>TTN</i> Truncating Variant CardiomyopathyParth N Patel, Kaoru Ito, Jon A L Willcox, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|June 13, 2018
A gene-centric strategy for identifying disease-causing rare variants in dilated cardiomyopathyClaire Horvat, Renee Johnson, Lien Lam, et al.
The New England Journal of Medicine|June 23, 2016
A Prospective Study of Sudden Cardiac Death among Children and Young AdultsRichard D Bagnall, Robert G Weintraub, Jodie Ingles, et al.
The New England Journal of Medicine|February 17, 2012
Truncations of titin causing dilated cardiomyopathyDaniel S Herman, Lien Lam, Matthew R G Taylor, et al.
Circulation. Genomic and Precision Medicine|December 29, 2022
Variant Location Is a Novel Risk Factor for Individuals With Arrhythmogenic Cardiomyopathy Due to a Desmoplakin (<i>DSP</i>) Truncating VariantEdgar T Hoorntje, Charlotte Burns, Luisa Marsili, et al.
Pageof 2