Identification of a novel frameshift mutation in the SCNN1B causing Liddle syndrome

Sci Bull (Beijing). 2023 Feb 26;68(4):383-387. doi: 10.1016/j.scib.2023.02.006. Epub 2023 Feb 7.
No abstract available

MeSH terms

  • Epithelial Sodium Channels / genetics
  • Frameshift Mutation / genetics
  • Humans
  • Hypertension* / genetics
  • Liddle Syndrome* / genetics

Substances

  • Epithelial Sodium Channels
  • SCNN1B protein, human