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.
Aldizkaria:
Endocrine

ISSN: 1559-0100,  1355-008X

Argitalpen urtea: 2023

Alea: 80

Zenbakia: 1

Orrialdeak: 47-53

Mota: Artikulua

DOI: 10.1007/S12020-022-03284-5 GOOGLE SCHOLAR
Datuen iturria: Scopus