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
32161960 (PubMed )
Supplement: hpaa037_suppl_supplementary_table_s2.doc
Liddle syndrome due to a novel mutation in the γ subunit of the epithelial sodium channel (ENaC) in family from Russia: a case report.
Kozina AA et al.
Bmc Nephrology, 2019
A Novel Frameshift Mutation of SCNN1G Causing Liddle Syndrome with Normokalemia.
Fan P et al.
American Journal of Hypertension, 2019
Molecular genetics of Liddle's syndrome.
Yang KQ et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry, 2014
Select a paper to view details