The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism

  1. Siffo, S.
  2. Gomes Pio, M.
  3. Martínez, E.B.
  4. Lachlan, K.
  5. Walker, J.
  6. Weill, J.
  7. González-Sarmiento, R.
  8. Rivolta, C.M.
  9. Targovnik, H.M.
Journal:
Endocrine

ISSN: 1559-0100,  1355-008X

Year of publication: 2023

Volume: 80

Issue: 1

Pages: 47-53

Type: Article

DOI: 10.1007/S12020-022-03284-5 GOOGLE SCHOLAR
Data source: Scopus