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Article

[Recurrent syncope related to catecholaminergic polymorphic ventricular tachycardia due to de novo RyR2-R2401H mutation].

Zhonghua xin xue guan bing za zhi - 25 Jan 2017

Liu X, Li J X, Hu J Z, Shen Y, Wan R, Xiong Q M, Zhou Q Q, Xie J Y, Jin J J, Yan X, Yu J H, Hong K

Abstract excerpt

Objective: To explore the clinical and molecular genetic features of a Chinese patient with catecholaminergic polymorphic ventricular tachycardia (CPVT). Methods: Clinical data including resting electrocardiography, echocardiography and treadmill exercise testing of a patient with CPVT admitted to our department in March 2013 were analyzed, and the peripheral venous blood samples of the patient and his family...

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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 28100344
DOI: 10.3760/cma.j.issn.0253-3758.2017.01.008

Genes

CALM1
CASQ2
TRDN
KCNJ2
RYR2

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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