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| 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 |
| Title : Next-Generation Sequencing Analysis Reveals Frequent Familial Origin and Oligogenism in Congenital Hypothyroidism With Dyshormonogenesis - Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
| Author(s) : Oliver-Petit I , Edouard T , Jacques V , Bournez M , Cartault A , Grunenwald S , Savagner F |
| Ref : Front Endocrinol (Lausanne) , 12 :657913 , 2021 |
| Abstract : Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
| ESTHER : Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
| PubMedSearch : Oliver-Petit_2021_Front.Endocrinol.(Lausanne)_12_657913 |
| PubMedID: 34248839 |