Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7

1. MacHiavelli, G.A.
2. Caputo, M.
3. Rivolta, C.M.
4. Olcese, M.C.
5. Gruñeiro-Papendieck, L.
6. Chiesa, A.
7. González-Sarmiento, R.
8. Targovnik, H.M.