Titlebook: Clinical Cardiogenetics; Hubert F. Baars,Pieter A. F. M. Doevendans,J. Pete Book 20162nd edition Springer International Publishing Switzer

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https://doi.org/10.1007/978-3-658-08575-9ventricular noncompaction. Indeed, an autosomal dominantly segregating cardiomyopathy has been described where a single sarcomere gene mutation caused idiopathic RCM in some and HCM in other family members [1].

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Christoph Seifarth,Frank L. Dederichsitochondrial disease..Cardiomyopathy, however, may be the first and only symptom. MELAS syndrome with hypertrophic cardiomyopathy and Kearns-Sayre syndrome with progressive conduction disorders are two examples of mitochondrial disease.

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Robotik in der Wirtschaftsinformatike last 20 years, major advances in clinical and mechanistic knowledge have provided very valuable information about the disease, but remaining questions still propel a large research activity on the subject. In this chapter, we review the present knowledge, on clinical, genetic, and molecular features of BrS.

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Introduction to Molecular Geneticsmilial cases, but with the recent developments of Next Generation Sequencing (NGS) also to identify genetic components involved in complex genetic cardiac diseases and to implement personalized genomics into routine patient care. In this introductory chapter several aspects of molecular genetics wil

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Hypertrophic Cardiomyopathys left ventricular hypertrophy (LVH) in the absence of abnormal loading conditions that may cause hypertrophy. The disease can present at any age and is highly variable in clinical expression. Patients can remain asymptomatic throughout their life, but HCM is also associated with premature mortality

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