Download PDF
Go back to website
If you have problems to see the content please click here
Other users also viewed these articles
Recommendations for the diagnosis and treatment of classic forms of 21-hydroxylase-deficient congenital adrenal hyperplasia
Amparo Rodríguez, Begoña Ezquieta, José Igancio Labarta, María Clemente, Rafael Espino, Amaia Rodriguez, Aranzazu Escribano
10.1016/j.anpede.2016.12.002
Congenital pachyonychia: A new case associated with the KRT17 gene
O. Micol-Martínez, V. López-González, P.W. Garcia-Marcos, T. Martínez-Menchón, E. Guillén-Navarro
10.1016/j.anpede.2015.08.013
Encephalopathy, kidney failure and retinopathy. CoQ10 deficiency due to COQ8B mutation
Victor Adam Lancet, Yolanda Romero Salas, María Luisa Justa Roldán, María Concepción García Jiménez, Gema Ariceta Iraola
10.1016/j.anpede.2020.05.008