Genetic diagnosis of X-linked dominant hypophosphatemic rickets in a cohort study: Tubular reabsorption of phosphate and 1,25(OH)2D serum levels are associated with PHEX mutation type

  1. Morey, M.
  2. Castro-Feijóo, L.
  3. Barreiro, J.
  4. Cabanas, P.
  5. Pombo, M.
  6. Gil, M.
  7. Bernabeu, I.
  8. Díaz-Grande, J.M.
  9. Rey-Cordo, L.
  10. Ariceta, G.
  11. Rica, I.
  12. Nieto, J.
  13. Vilalta, R.
  14. Martorell, L.
  15. Vila-Cots, J.
  16. Aleixandre, F.
  17. Fontalba, A.
  18. Soriano-Guillén, L.
  19. García-Sagredo, J.M.
  20. García-Miñaur, S.
  21. Rodríguez, B.
  22. Juaristi, S.
  23. García-Pardos, C.
  24. Martínez-Peinado, A.
  25. Millán, J.M.
  26. Medeira, A.
  27. Moldovan, O.
  28. Fernandez, A.
  29. Loidi, L.
  30. Show all authors +
Journal:
BMC Medical Genetics

ISSN: 1471-2350

Year of publication: 2011

Volume: 12

Type: Article

DOI: 10.1186/1471-2350-12-116 GOOGLE SCHOLAR lock_openOpen access editor