Evolution of a genetic diagnosis-Reference-Cited by-同舟云学术

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Evolution of a genetic diagnosis

Published:2013-12-20 Issue:6 Volume:86 Page:580-584
ISSN:0009-9163
Container-title:Clinical Genetics
language:en
Short-container-title:Clin Genet

Author:

Laksman Z.¹,Dulay D.²,Gollob M.H.³,Skanes A.C.⁴,Krahn A.D.⁵

Affiliation:

1. Department of Cardiac Electrophysiology; Western University; London Ontario Canada

2. Department of Cardiology; Heart Health Physicians; Victoria British Columbia Canada

3. Ottawa Heart Institute; University of Ottawa; Ottawa Ontario Canada

4. Department of Cardiology; Western University; London Ontario Canada

5. Department of Cardiology; University of British Columbia; Vancouver British Columbia Canada

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Reference16 articles.

1. Novel lamin A/C mutations in two families with dilated cardiomyopathy and conduction system disease;Jakobs;J Card Fail,2001

2. High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics;van Tintelen;Am Heart J,2007

3. Lamin A/C gene mutations in familial cardiomyopathy with advanced atrioventricular block and arrhythmia;Saga;Tohoku J Exp Med,2009

4. Genetic testing in heritable cardiac arrhythmia syndromes: differentiating pathogenic mutations from background genetic noise;Giudicessi;Curr Opin Cardiol,2013

5. Proof of “disease causing” mutation;Cotton;Hum Mutat,1998

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1. Overview of Molecular Quantification of the BCR-ABL Oncogene in CML Patients;Biosciences Biotechnology Research Asia;2022-09-29

2. Variant Reinterpretation in Survivors of Cardiac Arrest With Preserved Ejection Fraction (the Cardiac Arrest Survivors With Preserved Ejection Fraction Registry) by Clinicians and Clinical Commercial Laboratories;Circulation: Genomic and Precision Medicine;2021-06

3. Acute Management of Ventricular Arrhythmia in Patients With Suspected Inherited Heart Rhythm Disorders;JACC: Clinical Electrophysiology;2019-03

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