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Paper Details

LMNA Variants and Risk of Adult-Onset Cardiac Disease.
J Am Coll Cardiol
11
2022
Cardiac Disease, LMNA, LMNA Variants, LMNA variant, LMNA variants, arrhythmia, atrial fibrillation, bradyarrhythmia, cardiac disease, cardiomyopathy, dilated cardiomyopathy, heart failure, participants, person, ventricular arrhythmia
Author NameAffiliation
Seung Hoan ChoiBroad Institute of Harvard and the Massachusetts Institute of Technology
Seung Hoan ChoiBroad Institute of Harvard and the Massachusetts Institute of Technology
James P PirruccelloBroad Institute of Harvard and the Massachusetts Institute of Technology
Robert A HegeleSchulich School of Medicine and Dentistry, Western University, Canada Robarts Research Institute
Patrick T EllinorBroad Institute of Harvard and the Massachusetts Institute of Technology, USA Demoulas Center for Cardiac Arrhythmias, Massachusetts General Hospital
Patrick T EllinorBroad Institute of Harvard and the Massachusetts Institute of Technology, USA Demoulas Center for Cardiac Arrhythmias, Massachusetts General Hospital
Kathryn L Lunettaand Blood Institute and Boston University's Framingham Heart Study, Boston University School of Public Health
Steven A LubitzBroad Institute of Harvard and the Massachusetts Institute of Technology, USA Demoulas Center for Cardiac Arrhythmias, Massachusetts General Hospital
Steven A LubitzBroad Institute of Harvard and the Massachusetts Institute of Technology, USA Demoulas Center for Cardiac Arrhythmias, Massachusetts General Hospital
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Datasets

ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar is a freely accessible, public archive of submitted reports about the relationships among human variations and phenotypes, with supporting evidence.Link
ClinVarClinVar (https://www.ncbi.nlm.nih.gov/clinvar/) is a freely available, publLink