Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

  1. Laugel, V.
  2. Dalloz, C.
  3. Durand, M.
  4. Sauvanaud, F.
  5. Kristensen, U.
  6. Vincent, M.C.
  7. Pasquier, L.
  8. Odent, S.
  9. Cormier-Daire, V.
  10. Gener, B.
  11. Tobias, E.S.
  12. Tolmie, J.L.
  13. Martin-Coignard, D.
  14. Drouin-Garraud, V.
  15. Heron, D.
  16. Journel, H.
  17. Raffo, E.
  18. Vigneron, J.
  19. Lyonnet, S.
  20. Murday, V.
  21. Gubser-Mercati, D.
  22. Funalot, B.
  23. Brueton, L.
  24. Sanchez Del Pozo, J.
  25. Muñoz, E.
  26. Gennery, A.R.
  27. Salih, M.
  28. Noruzinia, M.
  29. Prescott, K.
  30. Ramos, L.
  31. Stark, Z.
  32. Fieggen, K.
  33. Chabrol, B.
  34. Sarda, P.
  35. Edery, P.
  36. Bloch-Zupan, A.
  37. Fawcett, H.
  38. Pham, D.
  39. Egly, J.M.
  40. Lehmann, A.R.
  41. Sarasin, A.
  42. Dollfus, H.
  43. Show all authors +
Journal:
Human Mutation

ISSN: 1059-7794 1098-1004

Year of publication: 2010

Volume: 31

Issue: 2

Pages: 113-126

Type: Review

DOI: 10.1002/HUMU.21154 GOOGLE SCHOLAR