Genotype-Phenotype Correlations in Apical Variant Hypertrophic Cardiomyopathy-Reference-Cited by-同舟云学术

Genotype-Phenotype Correlations in Apical Variant Hypertrophic Cardiomyopathy

Published:2014-12-14 Issue:3 Volume:10 Page:E139-E145
ISSN:1747-079X
Container-title:Congenital Heart Disease
language:en
Short-container-title:Congenit Heart Dis

Author:

Towe Eric C.¹,Bos J. Martijn²,Ommen Steve R.³,Gersh Bernard J.³,Ackerman Michael J.¹²³

Affiliation:

1. Department of Pediatrics; Division of Pediatric Cardiology; Mayo Clinic; Rochester Minn USA

2. Department of Molecular Pharmacology and Experimental Therapeutics; Windland Smith Rice Sudden Death Genomics Laboratory; Mayo Clinic; Rochester Minn USA

3. Department of Medicine; Division of Cardiovascular Diseases; Mayo Clinic; Rochester Minn USA

Publisher

Computers, Materials and Continua (Tech Science Press)

Subject

Cardiology and Cardiovascular Medicine,Radiology, Nuclear Medicine and imaging,General Medicine,Surgery,Pediatrics, Perinatology and Child Health

Reference17 articles.

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2. A molecular basis for familial hypertrophic cardiomyopathy: a beta cardiac myosin heavy chain gene missense mutation;Geisterfer-Lowrance;Cell,1990

3. Diagnostic, prognostic, and therapeutic implications of genetic testing for hypertrophic cardiomyopathy;Bos;J Am Coll Cardiol,2009

4. Echocardiography-guided genetic testing in hypertrophic cardiomyopathy: septal morphological features predict the presence of myofilament mutations;Binder;Mayo Clin Proc,2006

5. Apical hypertrophic cardiomyopathy;Ates;Tex Heart Inst J,2006

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