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
- Morey, M.
- Castro-Feijóo, L.
- Barreiro, J.
- Cabanas, P.
- Pombo, M.
- Gil, M.
- Bernabeu, I.
- Díaz-Grande, J.M.
- Rey-Cordo, L.
- Ariceta, G.
- Rica, I.
- Nieto, J.
- Vilalta, R.
- Martorell, L.
- Vila-Cots, J.
- Aleixandre, F.
- Fontalba, A.
- Soriano-Guillén, L.
- García-Sagredo, J.M.
- García-Miñaur, S.
- Rodríguez, B.
- Juaristi, S.
- García-Pardos, C.
- Martínez-Peinado, A.
- Millán, J.M.
- Medeira, A.
- Moldovan, O.
- Fernandez, A.
- Loidi, L.
- Show all authors +
Journal:
BMC Medical Genetics
ISSN: 1471-2350
Year of publication: 2011
Volume: 12
Type: Article