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Hereditary angioedema caused by a premature stop codon mutation in the SERPING1 gene.

Ying-Yang XuJian-Qing GuYu-Xiang Zhi
Published in: Clinical and translational allergy (2020)
Three known and six novel mutations in the SERPING1 gene were identified, and they produced a truncated nonfunctional C1 inhibitor without a reactive central loop. All the mutations led to reduced expression of SERPING1 mRNA in peripheral blood and low antigenic C1 inhibitor levels.
Keyphrases
  • peripheral blood
  • copy number
  • genome wide
  • poor prognosis
  • genome wide identification
  • binding protein
  • gene expression
  • angiotensin converting enzyme