A family with congenital hypothyroidism caused by a combination of loss-of-function mutations in the thyrotropin receptor and adenylate cyclase-stimulating G alpha-protein subunit genes
- Lado-Abeal, J.
- Castro-Piedras, I.
- Palos-Paz, F.
- Labarta-Aizpún, J.I.
- Albero-Gamboa, R.
ISSN: 1050-7256
Ano de publicación: 2011
Volume: 21
Número: 2
Páxinas: 103-109
Tipo: Artigo