Title : Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect - Bernal Barquero_2022_Int.J.Mol.Sci_23_9251 |
Author(s) : Bernal Barquero CE , Geysels RC , Jacques V , Carro GH , Martin M , Peyret V , Abregu MC , Papendieck P , Masini-Repiso AM , Savagner F , Chiesa AE , Citterio CE , Nicola JP |
Ref : Int J Mol Sci , 23 :9251 , 2022 |
Abstract : Bernal Barquero_2022_Int.J.Mol.Sci_23_9251 |
ESTHER : Bernal Barquero_2022_Int.J.Mol.Sci_23_9251 |
PubMedSearch : Bernal Barquero_2022_Int.J.Mol.Sci_23_9251 |
PubMedID: 36012511 |
Gene_locus related to this paper: human-TG |
Gene_locus related to this paper: human-TG |
Bernal Barquero CE, Geysels RC, Jacques V, Carro GH, Martin M, Peyret V, Abregu MC, Papendieck P, Masini-Repiso AM, Savagner F, Chiesa AE, Citterio CE, Nicola JP (2022)
Targeted Next-Generation Sequencing of Congenital Hypothyroidism-Causative Genes Reveals Unexpected Thyroglobulin Gene Variants in Patients with Iodide Transport Defect
Int J Mol Sci
23 :9251
Bernal Barquero CE, Geysels RC, Jacques V, Carro GH, Martin M, Peyret V, Abregu MC, Papendieck P, Masini-Repiso AM, Savagner F, Chiesa AE, Citterio CE, Nicola JP (2022)
Int J Mol Sci
23 :9251