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Journal of Clinical Hypertension (Greenwich, Conn.)|June 16, 2015
Prevalence of Liddle Syndrome Among Young Hypertension Patients of Undetermined Cause in a Chinese PopulationLin-Ping Wang, Kun-Qi Yang, Xiong-Jing Jiang, et al.Frontiers in Pediatrics|June 10, 2022
Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese FamilyDi Zhang, Yi Qu, Xue-Qi Dong, et al.Journal of Geriatric Cardiology : JGC|August 17, 2022
A novel missense mutation in obscurin gene in a Chinese consanguineous family with left ventricular noncompactionXue-Qi Dong, Pei-Pei Qin, Di Zhang, et al.Scientific Reports|May 27, 2017
A novel PRKAG2 mutation in a Chinese family with cardiac hypertrophy and ventricular pre-excitationKun-Qi Yang, Chao-Xia Lu, Ying Zhang, et al.Clinical and Experimental Hypertension (New York, N.Y. : 1993)|July 19, 2017
Genetic screening of SCNN1B and SCNN1G genes in early-onset hypertensive patients helps to identify Liddle syndromeKun-Qi Yang, Chao-Xia Lu, Peng Fan, et al.Journal of Geriatric Cardiology : JGC|May 16, 2022
Implication of a novel truncating mutation in titin as a cause of autosomal dominant left ventricular noncompactionXue-Qi Dong, Di Zhang, Yi Qu, et al.Frontiers in Pediatrics|July 18, 2022
Corrigendum: Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese FamilyDi Zhang, Yi Qu, Xue-Qi Dong, et al.American Journal of Hypertension|April 13, 2019
A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with NormokalemiaPeng Fan, Yu-Mo Zhao, Di Zhang, et al.Journal of Geriatric Cardiology : JGC|October 25, 2019
Anemia in patients with Takayasu arteritis: prevalence, clinical features, and treatmentYing Zhang, Di Zhang, Yi Qu, et al.American Journal of Hypertension|March 13, 2020
Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset HypertensionPeng Fan, Xiao-Cheng Pan, Di Zhang, et al.Pageof 5