Exploring digenic inheritance in arrhythmogenic cardiomyopathy

Background Arrhythmogenic cardiomyopathy (ACM) is an inherited genetic disorder, characterized by the substitution of heart muscle with fibro-fatty tissue and severe ventricular arrhythmias, often leading to heart failure and sudden cardiac death. ACM is considered a monogenic disorder, but the low...

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Vydáno v:	BMC medical genetics Ročník 18; číslo 1; s. 145 - 12
Hlavní autoři:	König, Eva, Volpato, Claudia Béu, Motta, Benedetta Maria, Blankenburg, Hagen, Picard, Anne, Pramstaller, Peter, Casella, Michela, Rauhe, Werner, Pompilio, Giulio, Meraviglia, Viviana, Domingues, Francisco S., Sommariva, Elena, Rossini, Alessandra
Médium:	Journal Article
Jazyk:	angličtina
Vydáno:	London BioMed Central 08.12.2017 BioMed Central Ltd BMC
Témata:	ACM Arrhythmia Arrhythmogenic cardiomyopathy Biomedical and Life Sciences Biomedicine Cardiomyopathy Clinical-Molecular Genetics and Cytogenetics Complications and side effects Cytogenetics Digenic inheritance Exome sequencing Gene Function Genetic aspects Genetic susceptibility Heart diseases Human Genetics Physiological aspects PKP2 Research Article Risk factors Italy Digenic inheritance PKP2 Arrhythmogenic cardiomyopathy ACM Exome sequencing
ISSN:	1471-2350, 1471-2350
On-line přístup:	Získat plný text
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