A new case of congenital goiter with hypothyroidism caused by a homozygous p.R277X mutation in the exon 7 of the thyroglobulin gene: A mutational hot spot could explain the recurrence of this mutation
- Rivolta, C.M.
- Moya, C.M.
- Gutnisky, V.J.
- Varela, V.
- Miralles-García, J.M.
- González-Sarmiento, R.
- Targovnik, H.M.
ISSN: 0021-972X
Ano de publicación: 2005
Volume: 90
Número: 6
Páxinas: 3766-3770
Tipo: Artigo