Associated Papers
Novel frameshift variant in the β subunit of epithelial sodium channels uncovers Liddle syndrome in a young patient with metabolic syndrome: a case report with review of literature.
Li A et al.
Endocrine Journal, 2026
A Novel Frame-Shift Mutation in SCNN1B Identified in a Chinese Family Characterized by Early-Onset Hypertension.
Lu YT et al.
Frontiers in Cardiovascular Medicine, 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
32161960 (PubMed )
Supplement: hpaa037_suppl_supplementary_table_s2.doc
Liddle Syndrome: Review of the Literature and Description of a New Case.
Tetti M et al.
International Journal of Molecular Sciences, 2018
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