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| 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 |
| Title : Two novel mutations in the thyroglobulin gene as cause of congenital hypothyroidism: identification a cryptic donor splice site in the exon 19 - Targovnik_2012_Mol.Cell.Endocrinol_348_313 |
| Author(s) : Targovnik HM , Edouard T , Varela V , Tauber M , Citterio CE , Gonzalez-Sarmiento R , Rivolta CM |
| Ref : Mol Cell Endocrinol , 348 :313 , 2012 |
| Abstract : Targovnik_2012_Mol.Cell.Endocrinol_348_313 |
| ESTHER : Targovnik_2012_Mol.Cell.Endocrinol_348_313 |
| PubMedSearch : Targovnik_2012_Mol.Cell.Endocrinol_348_313 |
| PubMedID: 21958696 |
| Gene_locus related to this paper: human-TG |