Gender Differences in the Inheritance Mode of RYR2 Mutations in Catecholaminergic Polymorphic Ventricular Tachycardia Patients

Catecholaminergic polymorphic ventricular tachycardia (CPVT) is one of the causes of sudden cardiac death in young people and results from RYR2 mutations in ~60% of CPVT patients. The inheritance of the RYR2 mutations follows an autosomal dominant trait, however, de novo mutations are often identifi...

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Bibliographic Details
Published in:PLoS One
Main Authors: Ohno, Seiko, Hasegawa, Kanae, Horie, Minoru
Format: Artigo
Language:Inglês
Published: Public Library of Science 2015
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Research Article
Online Access:https://ncbi.nlm.nih.gov/pmc/articles/PMC4482545/
https://ncbi.nlm.nih.gov/pubmed/26114861
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0131517
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