Novel mutational mechanism in the thyroglobulin gene: Imperfect DNA inversion as a cause for hereditary hypothyroidism

  1. Citterio, C.E.
  2. Rossetti, L.C.
  3. Souchon, P.F.
  4. Morales, C.
  5. Thouvard-Viprey, M.
  6. Salmon-Musial, A.S.
  7. Mauran, P.L.A.
  8. Doco-Fenzy, M.
  9. González-Sarmiento, R.
  10. Rivolta, C.M.
  11. De Brasi, C.D.
  12. Targovnik, H.M.
Journal:
Molecular and Cellular Endocrinology

ISSN: 0303-7207 1872-8057

Year of publication: 2013

Volume: 381

Issue: 1-2

Pages: 220-229

Type: Article

DOI: 10.1016/J.MCE.2013.07.034 GOOGLE SCHOLAR