Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease

  1. Gago-Díaz, M.
  2. Blanco-Verea, A.
  3. Teixidó-Turà, G.
  4. Valenzuela, I.
  5. Del Campo, M.
  6. Borregan, M.
  7. Sobrino, B.
  8. Amigo, J.
  9. García-Dorado, D.
  10. Evangelista, A.
  11. Carracedo, T.
  12. Brion, M.
Journal:
Clinica Chimica Acta

ISSN: 1873-3492 0009-8981

Year of publication: 2014

Volume: 437

Pages: 88-92

Type: Article

DOI: 10.1016/J.CCA.2014.07.016 GOOGLE SCHOLAR

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