FOSL2 truncating variants in the last exon cause a neurodevelopmental disorder with scalp and enamel defects

  1. Cospain, A.
  2. Rivera-Barahona, A.
  3. Dumontet, E.
  4. Gener, B.
  5. Bailleul-Forestier, I.
  6. Meyts, I.
  7. Jouret, G.
  8. Isidor, B.
  9. Brewer, C.
  10. Wuyts, W.
  11. Moens, L.
  12. Delafontaine, S.
  13. Keung Lam, W.W.
  14. Van Den Bogaert, K.
  15. Boogaerts, A.
  16. Scalais, E.
  17. Besnard, T.
  18. Cogne, B.
  19. Guissard, C.
  20. Rollier, P.
  21. Carre, W.
  22. Bouvet, R.
  23. Tarte, K.
  24. Gómez-Carmona, R.
  25. Lapunzina, P.
  26. Odent, S.
  27. Faoucher, M.
  28. Dubourg, C.
  29. Ruiz-Pérez, V.L.
  30. Devriendt, K.
  31. Pasquier, L.
  32. Pérez-Jurado, L.A.
  33. Show all authors +
Journal:
Genetics in Medicine

ISSN: 1530-0366 1098-3600

Year of publication: 2022

Volume: 24

Issue: 12

Pages: 2475-2486

Type: Article

DOI: 10.1016/J.GIM.2022.09.002 GOOGLE SCHOLAR

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