The FXII c.-4T>C Polymorphism as a Disease Modifier in Patients With Hereditary Angioedema Due to the FXII p.Thr328Lys Variant

  1. Corvillo, F.
  2. Morena-Barrio, M.E.D.L.
  3. Marcos-Bravo, C.
  4. López-Trascasa, M.
  5. Vicente, V.
  6. Emsley, J.
  7. Caballero, T.
  8. Corral, J.
  9. López-Lera, A.
Journal:
Frontiers in Genetics

ISSN: 1664-8021

Year of publication: 2020

Volume: 11

Type: Article

DOI: 10.3389/FGENE.2020.01033 GOOGLE SCHOLAR lock_openOpen access editor
Data source: Scopus