Origin of the mutations in the parkin gene in Europe: Exon rearrangements are independent recurrent events, whereas point mutations may result from founder effects

  1. Periquet, M.
  2. Lücking, C.B.
  3. Vaughan, J.R.
  4. Bonifati, V.
  5. ürr, A.
  6. De Michele, G.
  7. Horstink, M.W.
  8. Farrer, M.
  9. Illarioshkin, S.N.
  10. Pollak, P.
  11. Borg, M.
  12. Brefel-Courbon, C.
  13. Denefle, P.
  14. Gasser, T.
  15. Gasser, T.
  16. Breteler, M.M.B.
  17. Wood, N.W.
  18. Agid, Y.
  19. Brice, A.
  20. Bonnet, A.-M.
  21. Borg, M.
  22. Brice, A.
  23. Destée, A.
  24. Dürr, F.
  25. Durif, F.
  26. Feingold, J.
  27. Fénelon, G.
  28. Gasparini, F.
  29. Martinez, M.
  30. Penet, C.
  31. Pollak, P.
  32. Rascol, O.
  33. Tison, F.
  34. Tranchant, C.
  35. Vérin, M.
  36. Viallet, F.
  37. Vidailhet, M.
  38. Warter, J.-M.
  39. Vaughan, J.R.
  40. Brice, A.
  41. Dürr, A.
  42. Martinez, M.
  43. Gasser, T.
  44. Müller-Myhsok, B.
  45. Breteler, M.
  46. Harhangi, S.
  47. Oostra, B.
  48. Bonifati, M.
  49. DeMari, M.
  50. Fabrizio, E.
  51. Filla, A.
  52. Meco, G.
  53. Erakutsi egile guztiak +
Aldizkaria:
American Journal of Human Genetics

ISSN: 0002-9297

Argitalpen urtea: 2001

Alea: 68

Zenbakia: 3

Orrialdeak: 617-626

Mota: Artikulua

DOI: 10.1086/318791 GOOGLE SCHOLAR lock_openSarbide irekia editor
Datuen iturria: Scopus