| Title : The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism - Siffo_2023_Endocrine_80_47 |
| Author(s) : Siffo S , Gomes Pio M , Martinez EB , Lachlan K , Walker J , Weill J , Gonzalez-Sarmiento R , Rivolta CM , Targovnik HM |
| Ref : Endocrine , 80 :47 , 2023 |
| Abstract : Siffo_2023_Endocrine_80_47 |
| ESTHER : Siffo_2023_Endocrine_80_47 |
| PubMedSearch : Siffo_2023_Endocrine_80_47 |
| PubMedID: 36547798 |
Siffo S, Gomes Pio M, Martinez EB, Lachlan K, Walker J, Weill J, Gonzalez-Sarmiento R, Rivolta CM, Targovnik HM (2023)
The p.Pro2232Leu variant in the ChEL domain of thyroglobulin gene causes intracellular transport disorder and congenital hypothyroidism
Endocrine
80 :47
Siffo S, Gomes Pio M, Martinez EB, Lachlan K, Walker J, Weill J, Gonzalez-Sarmiento R, Rivolta CM, Targovnik HM (2023)
Endocrine
80 :47