Identification of <i>SCN5a</i> p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease

Identification of <i>SCN5a</i> p.C335R Variant in a Large Family with Dilated Cardiomyopathy and Conduction Disease

Introduction: Familial dilated cardiomyopathy (DCM) is clinically variable and has been associated with mutations in more than 50 genes. Rapid improvements in DNA sequencing have led to the identification of diverse rare variants with unknown significance (VUS), which underlines the importance of fu...

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Bibliographic Details
Main Authors: Farbod Sedaghat-Hamedani, Sabine Rebs, Ibrahim El-Battrawy, Safak Chasan, Tobias Krause, Jan Haas, Rujia Zhong, Zhenxing Liao, Qiang Xu, Xiaobo Zhou, Ibrahim Akin, Edgar Zitron, Norbert Frey, Katrin Streckfuss-Bömeke, Elham Kayvanpour
Format: Article
Language:English
Published: MDPI AG 2021-11-01
Series:International Journal of Molecular Sciences
Subjects:
familial DCM
<i>SCN5a</i>
conduction disease
Online Access:https://www.mdpi.com/1422-0067/22/23/12990

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