Download PDF

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