Article
Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations
Fecha
2014Registro en:
RAMOS, H. E. et al. Extreme phenotypic variability of thyroid dysgenesis in six new cases of congenital hypothyroidism due to PAX8 gene loss-of-function mutations. European Journal of Endocrinology, v. 171, p. 499–507, 2014.
0804-4643
10.1530/EJE-13-1006
Autor
Ramos, Helton Estrela
Carré, A
Chevrier, L
Szinnai, G
Tron, E
Cerqueira, Taíse Lima de Oliveira
Léger, J
Cabrol, S
Puel, O
Queinnec, C
De Roux, N
Guillot, L
Castanet, M
Polak, M