Liddle Syndrome due to a Novel c.1713 Deletion in the Epithelial Sodium Channel β-Subunit in a Normotensive Adolescent
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Elsevier BV
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1. Low renin forms of monogenic hypertension: review of the evidence;Journal of Clinical Medicine of Kazakhstan;2024-02-25
2. Reverse Phenotypes of Patients with Genetically Confirmed Liddle Syndrome;Clinical Journal of the American Society of Nephrology;2024-01-24
3. Clinical Features and Mutations in Children with Liddle Syndrome: A Systematic Review of Case Reports;Indian Pediatrics Case Reports;2024-01
4. A frameshift mutation in the SCNN1B gene in a family with Liddle syndrome: A case report and systematic review;Molecular Medicine Reports;2023-12-08
5. Mineralocorticoid excess;Steroids in the Laboratory and Clinical Practice;2023
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