Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: Identification a cryptic donor splice site in the exon 19

1. Targovnik, H.M.
2. Edouard, T.
3. Varela, V.
4. Tauber, M.
5. Citterio, C.E.
6. González-Sarmiento, R.
7. Rivolta, C.M.