Associated Papers
A Family with Liddle Syndrome Caused by a Novel Stop-Gain Mutation in the γ Subunit of Epithelial Sodium Channels.
Wang X et al.
Nephron, 2022
Pathogenicity and Long-Term Outcomes of Liddle Syndrome Caused by a Nonsense Mutation of SCNN1G in a Chinese Family.
Zhang D et al.
Frontiers in Pediatrics, 2022
Pediatric Liddle Syndrome Caused by a Novel SCNN1G Variant in a Chinese Family and Characterized by Early-Onset Hypertension.
Fan P et al.
American Journal of Hypertension, 2020
Whole-Exome Sequencing in Adults With Chronic Kidney Disease: A Pilot Study.
Lata S et al.
Annals of Internal Medicine, 2018
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