Xue-qi Dong

Chinese Academy Of Medical Sciences And Peking Union Medical College
Beijing, China

Last Updated: 09/26/2026

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Found 8 publications

A novel missense mutation in obscurin gene in a Chinese consanguineous family with left ventricular noncompaction.

A novel missense mutation in obscurin gene in a Chinese consanguineous family with left ventricular noncompaction.

Journal: Journal of geriatric cardiology : JGC

Published: August 17, 2022

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Journal: Frontiers in pediatrics

Published: June 05, 2022

Implication of a novel truncating mutation in titin as a cause of autosomal dominant left ventricular noncompaction.

Implication of a novel truncating mutation in titin as a cause of autosomal dominant left ventricular noncompaction.

Journal: Journal of geriatric cardiology : JGC

Published: May 16, 2022

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.

Journal: Frontiers in pediatrics

Published: March 01, 2022

Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension.

Identification of NF1 Frameshift Variants in Two Chinese Families With Neurofibromatosis Type 1 and Early-Onset Hypertension.

Journal: Frontiers in pediatrics

Published: September 29, 2021

A narrative review of prehypertension and the cardiovascular system: effects and potential pathogenic mechanisms.

A narrative review of prehypertension and the cardiovascular system: effects and potential pathogenic mechanisms.

Journal: Annals of translational medicine

Published: February 11, 2021

A novel phenotype with splicing mutation identified in a Chinese family with desminopathy.

A novel phenotype with splicing mutation identified in a Chinese family with desminopathy.

Journal: Chinese medical journal

Published: January 08, 2019

Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.

Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndrome.

Journal: Clinical and experimental hypertension (New York, N.Y. : 1993)

Published: July 19, 2017

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Last Updated: 09/26/2026