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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Detalles Bibliográficos
Autores principales: Ohno, Seiko, Hasegawa, Kanae, Horie, Minoru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482545/
https://www.ncbi.nlm.nih.gov/pubmed/26114861
http://dx.doi.org/10.1371/journal.pone.0131517

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4482545/
https://www.ncbi.nlm.nih.gov/pubmed/26114861
http://dx.doi.org/10.1371/journal.pone.0131517

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