RYR2 Sequencing Reveals Novel Missense Mutations in a Kazakh Idiopathic Ventricular Tachycardia Study Cohort-Reference-Cited by-同舟云学术

RYR2 Sequencing Reveals Novel Missense Mutations in a Kazakh Idiopathic Ventricular Tachycardia Study Cohort

Published:2014-06-30 Issue:6 Volume:9 Page:e101059
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Akilzhanova Ainur,Guelly Christian,Nuralinov Omirbek,Nurkina Zhannur,Nazhat Dinara,Smagulov Shalkhar,Tursunbekov Azat,Alzhanova Anar,Rashbayeva Gulzhaina,Abdrakhmanov Ayan,Dosmagambet Sholpan,Trajanoski Slave,Zhumadilov Zhaxybay,Sharman Almaz,Bekbosynova Mahabbat

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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3. Correction: “Ryanopathies” and RyR2 dysfunctions: can we further decipher them using in vitro human disease models?;Cell Death & Disease;2022-11-30

4. Patients with coronary heart disease, dilated cardiomyopathy and idiopathic ventricular tachycardia share overlapping patterns of pathogenic variation in cardiac risk genes;PeerJ;2021-01-19

5. Ethnicity and the risk of ventricular arrhythmias due to stable ischemic heart disease;Journal of Clinical Medicine of Kazakhstan;2017-03-15