Novel compound heterozygous Thyroglobulin mutations c.745+1G>A/c.7036+2T>A associated with congenital goiter and hypothyroidism in a Vietnamese family. Identification of a new cryptic 5' splice site in the exon 6

1. Citterio, C.E.
2. Morales, C.M.
3. Bouhours-Nouet, N.
4. Machiavelli, G.A.
5. Bueno, E.
6. Gatelais, F.
7. Coutant, R.
8. González-Sarmiento, R.
9. Rivolta, C.M.
10. Targovnik, H.M.