A rare P2X7 variant Arg307Gln with absent pore formation function protects against neuroinflammation in multiple sclerosis

  1. Gu, B.J.
  2. Field, J.
  3. Dutertre, S.
  4. Ou, A.
  5. Kilpatrick, T.J.
  6. Lechner-Scott, J.
  7. Scott, R.
  8. Lea, R.
  9. Taylor, B.V.
  10. Stankovich, J.
  11. Butzkueven, H.
  12. Gresle, M.
  13. Laws, S.M.
  14. Petrou, S.
  15. Hoffjan, S.
  16. Akkad, D.A.
  17. Graham, C.A.
  18. Hawkins, S.
  19. Glaser, A.
  20. Bedri, S.K.
  21. Hillert, J.
  22. Matute, C.
  23. Antiguedad, A.
  24. Wiley, J.S.
  25. Baxter, A.G.
  26. Kermode, A.G.
  27. Booth, D.R.
  28. Mason, D.F.
  29. Stewart, G.J.
  30. Charlesworth, J.C.
  31. Tajouri, L.
  32. Griffiths, L.R.
  33. Slee, M.
  34. Brown, M.A.
  35. Moscato, P.
  36. Broadley, S.A.
  37. Vucic, S.
  38. Carrol, W.M.
  39. Barnett, M.H.
  40. Show all authors +
Journal:
Human Molecular Genetics

ISSN: 1460-2083,  0964-6906

Year of publication: 2015

Volume: 24

Issue: 19

Pages: 5644-5654

Type: Article

DOI: 10.1093/HMG/DDV278 GOOGLE SCHOLAR lock_openOpen access editor

Sustainable development goals

Data source: Scopus