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.
Revue:
Endocrine

ISSN: 1559-0100,  1355-008X

Année de publication: 2023

Volumen: 80

Número: 1

Pages: 47-53

Type: Article

DOI: 10.1007/S12020-022-03284-5 GOOGLE SCHOLAR
La source de données: Scopus