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
Titel:
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
Auteur:
Morey, Marcos Castro-Feijóo, Lidia Barreiro, Jesús Cabanas, Paloma Pombo, Manuel Gil, Marta Bernabeu, Ignacio Díaz-Grande, José M Rey-Cordo, Lourdes Ariceta, Gema Rica, Itxaso Nieto, José Vilalta, Ramón Martorell, Loreto Vila-Cots, Jaime Aleixandre, Fernando Fontalba, Ana Soriano-Guillén, Leandro García-Sagredo, José M García-Miñaur, Sixto Rodríguez, Berta Juaristi, Saioa García-Pardos, Carmen Martínez-Peinado, Antonio Millán, José M Medeira, Ana Moldovan, Oana Fernandez, Angeles Loidi, Lourdes