Qiqing Sun
Zhengzhou, China
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 9 publications
A case of polyglucosan body myopathy caused by an RBCK1 gene variant and literature review.
Journal: Molecular genetics & genomic medicine
Published: November 24, 2023
Clinical and genetic analysis of eight children with Primary hypertrophic cardiomyopathy
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: September 20, 2023
Bisphenol B induces developmental toxicity in zebrafish via oxidative stress.
Journal: Environmental science and pollution research international
Published: August 16, 2023
Clinical and genetic analysis of five children with Catecholaminergic polymorphic ventricular tachycardia due to variants of RYR2 gene
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 02, 2023
Genetic analysis of a child with restricted cardiomyopathy and phenylketonuria and a literature review
Journal: Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics
Published: August 02, 2023
Case report of a child with long QT syndrome type 14 caused by CALM1 gene mutation and literature review.
Journal: Molecular genetics & genomic medicine
Published: April 28, 2023
Cardiomyopathy in children: a single-centre, retrospective study of genetic and clinical characteristics.
Journal: BMJ paediatrics open
Published: April 12, 2023
Identification of a novel variant in N-cadherin associated with dilated cardiomyopathy.
Journal: Frontiers in medicine
Published: May 16, 2022
Whole-exome sequencing reveals two de novo variants in the RBM20 gene in two Chinese patients with left ventricular non-compaction cardiomyopathy.
Journal: Pediatric investigation
Published: August 20, 2019
Showing 1-9 of 9
Last Updated: 09/26/2026