In the last decade, genetics has been emerging as a primary issue
in the diagnosis and management of cardiomyopathies. This book is
intended to be a state-of-the-art monograph on these diseases,
describing their genetic causes, defining the molecular basis and
presenting extensive descriptions of genotype-phenotype
correlations. Other chapters are focused on the role of clinical
observation, on ECG and echocardiography. With its highlight on the
most recent discoveries in the field of molecular genetics as well
as on the correct clinical approach to patients with heart muscle
disease, the book is aimed at physicians and clinical cardiologists
with a particular interest in myocardial diseases and in their
genetic causes.
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