Erratum: Missense Mutations of the Pro65 Residue of PCGF2 Cause a Recognizable Syndrome Associated with Craniofacial, Neurological, Cardiovascular, and Skeletal Features (The American Journal of Human Genetics (2018) 103(5) (786–793), (S0002929718303239), (10.1016/j.ajhg.2018.09.012))

  1. Turnpenny, P.D.
  2. Wright, M.J.
  3. Sloman, M.
  4. Caswell, R.
  5. van Essen, A.J.
  6. Gerkes, E.
  7. Pfundt, R.
  8. White, S.M.
  9. Shaul-Lotan, N.
  10. Carpenter, L.
  11. Schaefer, G.B.
  12. Fryer, A.
  13. Innes, A.M.
  14. Forbes, K.P.
  15. Chung, W.K.
  16. McLaughlin, H.
  17. Henderson, L.B.
  18. Roberts, A.E.
  19. Heath, K.E.
  20. Paumard-Hernández, B.
  21. Gener, B.
  22. Fawcett, K.A.
  23. Gjergja-Juraški, R.
  24. Pilz, D.T.
  25. Fry, A.E.
Revue:
American Journal of Human Genetics

ISSN: 1537-6605,  0002-9297

Année de publication: 2018

Volumen: 103

Número: 6

Pages: 1054-1055

Type: Erreur

DOI: 10.1016/J.AJHG.2018.11.009 GOOGLE SCHOLAR lock_openAccès ouvert editor

Objectifs de Développement Durable

La source de données: Scopus