Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain

  1. Estalella, I.
  2. Rica, I.
  3. De Nanclares, G.P.
  4. Bilbao, J.R.
  5. Vazquez, J.A.
  6. San Pedro, J.I.
  7. Busturia, M.A.
  8. Castaño, L.
  9. Abellán, M.
  10. Espiga, J.
  11. López-Capapé, M.
  12. Unanue, G.
  13. Fernández, C.
  14. Sobradillo, B.
  15. Tapia, L.
  16. Rivas, F.
  17. Prieto, J.
  18. López, M.J.
  19. Bueno, G.
  20. Cortazar, A.
  21. Gaztambide, S.
  22. Martul, P.
  23. Vázquez, F.
  24. Vela, A.
  25. Reig, C.
  26. Borrás, V.
  27. Rodríguez-Rigual, M.
  28. Casas, J.
  29. Gómez Vida, J.
  30. Menéndez, E.
  31. Luengo, J.L.
  32. Barrio, R.
  33. Garcia-Cuartero, B.
  34. Bel, J.
  35. Rodríguez, A.
  36. Ruiz-Cano, R.
  37. Jiménez-Bustos, J.M.
  38. Barreiro, J.
  39. Hermoso, F.
  40. Luzuriaga, C.
  41. Diaz De Greñu, C.
  42. Espino, R.
  43. Oyarzabal, M.
  44. Gómez-Gila A., null
  45. Show all authors +
Journal:
Clinical Endocrinology

ISSN: 0300-0664 1365-2265

Year of publication: 2007

Volume: 67

Issue: 4

Pages: 538-546

Type: Article

DOI: 10.1111/J.1365-2265.2007.02921.X GOOGLE SCHOLAR

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