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. Erakutsi egile guztiak +
Aldizkaria:
Human Molecular Genetics

ISSN: 1460-2083,  0964-6906

Argitalpen urtea: 2015

Alea: 24

Zenbakia: 19

Orrialdeak: 5644-5654

Mota: Artikulua

DOI: 10.1093/HMG/DDV278 GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus