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

  1. Lado-Abeal, J.
  2. Castro-Piedras, I.
  3. Palos-Paz, F.
  4. Labarta-Aizpún, J.I.
  5. Albero-Gamboa, R.
Zeitschrift:
Thyroid

ISSN: 1050-7256

Datum der Publikation: 2011

Ausgabe: 21

Nummer: 2

Seiten: 103-109

Art: Artikel

DOI: 10.1089/THY.2010.0187 GOOGLE SCHOLAR