Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema

N. Nagy, Malcolm W. Greaves, Akio Tanaka, John A. McGrath, Clive E. Grattan

Research output: Contribution to journalArticle

18 Citations (Scopus)
Original languageEnglish
Pages (from-to)62-64
Number of pages3
JournalJournal of Dermatological Science
Volume56
Issue number1
DOIs
Publication statusPublished - Oct 2009

Fingerprint

Complement C1 Inactivator Proteins
Hereditary Angioedema Type III
Hereditary Angioedemas
Factor XII
Inborn Genetic Diseases
Kallikreins
Bradykinin
Missense Mutation
Amino Acid Substitution
Pedigree
Exons
Edema
Skin
Genes
United Kingdom

Keywords

  • Bradykinin
  • Coagulation factor XII
  • Genetic disease
  • Oedema
  • Skin

ASJC Scopus subject areas

  • Dermatology
  • Biochemistry
  • Molecular Biology

Cite this

Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema. / Nagy, N.; Greaves, Malcolm W.; Tanaka, Akio; McGrath, John A.; Grattan, Clive E.

In: Journal of Dermatological Science, Vol. 56, No. 1, 10.2009, p. 62-64.

Research output: Contribution to journalArticle

Nagy, N. ; Greaves, Malcolm W. ; Tanaka, Akio ; McGrath, John A. ; Grattan, Clive E. / Recurrent European missense mutation in the F12 gene in a British family with type III hereditary angioedema. In: Journal of Dermatological Science. 2009 ; Vol. 56, No. 1. pp. 62-64.
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