A Novel Splicing Mutation in the ACVRL1/ALK1 Gene as a Cause of HHT2

  1. Díaz, S.E.
  2. Peñalva, M.
  3. Recio-Poveda, L.
  4. Vilches, S.
  5. Casado-Vela, J.
  6. Pérez, J.P.
  7. Botella, L.M.
  8. Albiñana, V.
  9. Cuesta, A.M.
Journal:
Journal of Clinical Medicine

ISSN: 2077-0383

Year of publication: 2022

Volume: 11

Issue: 11

Type: Article

DOI: 10.3390/JCM11113053 GOOGLE SCHOLAR lock_openOpen access editor
Data source: Scopus