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

Bernabeu Morón, Ignacio; Loidi Fernández, Lourdes; Pombo Arias, Manuel; Cabanas Rodríguez, Paloma; Castro Feijoo, Lidia; Barreiro Conde, Jesús; Gil Calvo, Marta; Morey Villar, Marcos; Rodríguez Sánchez, Berta; Rey Cordo, Carmen Lourdes
Thumbnail
Statistics
Statistics
Identifiers
Identifiers
URI: http://hdl.handle.net/20.500.11940/5774
PMID: 21902834
ISSN: 1471-2350
Full record
Services
Services
RISMendeleyLinksolver
Date issued
2011
Journal title
BMC Medical Genetics
Type of content
Artigo