Titlebook: Genetic Cardiomyopathies; A Clinical Approach Gianfranco Sinagra (Professor of Cardiology Chief Book 2013 Springer-Verlag Italia 2013 Card

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Julietta Raymond,Ruth D. J. Alberted are not surprising, considering that in these diseases the defective gene is expressed in different structures or tissues. This is for example the case in the mitochondrial genes where production of abnormal proteins can cause multiform tissue abnormalities and/or dysfunction of different organs.

Mast-Cell

ANIM

,The Role of Clinical Observation: Red Flag 4 — Cardiomyopathies and Sensorineural Hearing Loss,fected patients. Sch?nberger et al. [.] considered the gene encoding epicardin (a transcription factor expressed in the myocardium and the cochlea) to be a candidate gene, but a specific mutation was not identified. In a later study, Sch?nberger et al. [.] found a deletion in the . gene, which was p

Cholesterol

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Concluding Remarks,functional (arrhythmogenic right ventricular cardiomyopathy [ARVC]). In 2006 [.], the American Heart Association suggested an approach that was based mainly on etiology (genetic, mixed, acquired) and considered two groups: primary CMPs (the disease is solely or predominantly localized in the heart)

FOVEA

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https://doi.org/10.1007/978-3-031-66906-4d by the clinical cardiologist in this emerging medical field, in which the goal is to provide a precise diagnosis, stratify the risk and treat patients correctly, and advise them on personal and family choices.

善變

Designing Current-Carrying Connections,fected patients. Sch?nberger et al. [.] considered the gene encoding epicardin (a transcription factor expressed in the myocardium and the cochlea) to be a candidate gene, but a specific mutation was not identified. In a later study, Sch?nberger et al. [.] found a deletion in the . gene, which was p

GREG

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Nikolaos Stylos,Roya Rahimi,Peter Robinsonfunctional (arrhythmogenic right ventricular cardiomyopathy [ARVC]). In 2006 [.], the American Heart Association suggested an approach that was based mainly on etiology (genetic, mixed, acquired) and considered two groups: primary CMPs (the disease is solely or predominantly localized in the heart)