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
Liddle syndrome with a SCNN1B mutation: a case report and systematic review.
Tang Q et al.
Bmc Nephrology, 2025
A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review.
Lu Y et al.
Molecular Medicine Reports, 2024
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
Liddle syndrome: clinical and genetic profiles.
Cui Y et al.
Journal of Clinical Hypertension (greenwich, Conn.), 2017
Select a paper to view details