Molecular analysis of congenital goitres with hypothyroidism caused by defective thyroglobulin synthesis. Identification of a novel c.7006C>T [p.R2317X] mutation and expression of minigenes containing nonsense mutations in exon 7

  1. MacHiavelli, G.A.
  2. Caputo, M.
  3. Rivolta, C.M.
  4. Olcese, M.C.
  5. Gruñeiro-Papendieck, L.
  6. Chiesa, A.
  7. González-Sarmiento, R.
  8. Targovnik, H.M.
Journal:
Clinical Endocrinology

ISSN: 0300-0664 1365-2265

Year of publication: 2010

Volume: 72

Issue: 1

Pages: 112-121

Type: Article

DOI: 10.1111/J.1365-2265.2009.03621.X GOOGLE SCHOLAR