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
- Citterio, C.E.
- Morales, C.M.
- Bouhours-Nouet, N.
- Machiavelli, G.A.
- Bueno, E.
- Gatelais, F.
- Coutant, R.
- González-Sarmiento, R.
- Rivolta, C.M.
- Targovnik, H.M.
ISSN: 1872-8057, 0303-7207
Ano de publicación: 2015
Volume: 404
Páxinas: 102-112
Tipo: Artigo