- Tytuł:
-
A frameshift mutation in the SCNN1B gene in a family with
Liddle syndrome : A case report and systematic review. - Autorzy:
- Źródło:
- Molecular medicine reports [Mol Med Rep] 2024 Feb; Vol. 29 (2). Date of Electronic Publication: 2023 Dec 15.
- Typ publikacji:
- Case Reports; Systematic Review; Journal Article
- MeSH Terms:
-
Liddle Syndrome */diagnosisLiddle Syndrome */geneticsLiddle Syndrome */drug therapy
Hypertension*/genetics
Hypertension*/drug therapy
Humans ; Epithelial Sodium Channels/genetics ; Frameshift Mutation ; Mutation ; Potassium
Czasopismo naukowe