Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing

  1. Calmels, N.
  2. Greff, G.
  3. Obringer, C.
  4. Kempf, N.
  5. Gasnier, C.
  6. Tarabeux, J.
  7. Miguet, M.
  8. Baujat, G.
  9. Bessis, D.
  10. Bretones, P.
  11. Cavau, A.
  12. Digeon, B.
  13. Doco-Fenzy, M.
  14. Doray, B.
  15. Feillet, F.
  16. Gardeazabal, J.
  17. Gener, B.
  18. Julia, S.
  19. Llano-Rivas, I.
  20. Mazur, A.
  21. Michot, C.
  22. Renaldo-Robin, F.
  23. Rossi, M.
  24. Sabouraud, P.
  25. Keren, B.
  26. Depienne, C.
  27. Muller, J.
  28. Mandel, J.-L.
  29. Laugel, V.
  30. Show all authors +
Journal:
Orphanet Journal of Rare Diseases

ISSN: 1750-1172

Year of publication: 2016

Volume: 11

Issue: 1

Type: Article

DOI: 10.1186/S13023-016-0408-0 GOOGLE SCHOLAR lock_openOpen access editor
Data source: Scopus