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| Title : Insertion of an Alu Element in Thyroglobulin Gene as a Novel Cause of Congenital Hypothyroidism - Bruellman_2020_Thyroid__ |
| Author(s) : Bruellman R , Watanabe Y , Shareef R , Abdullah MA , Dumitrescu A , Strauss BS , Refetoff S , Weiss RE |
| Ref : Thyroid , : , 2020 |
| Abstract : Bruellman_2020_Thyroid__ |
| ESTHER : Bruellman_2020_Thyroid__ |
| PubMedSearch : Bruellman_2020_Thyroid__ |
| PubMedID: 31868128 |
| Title : A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report - Watanabe_2018_BMC.Med.Genet_19_69 |
| Author(s) : Watanabe Y , Sharwood E , Goodwin B , Creech MK , Hassan HY , Netea MG , Jaeger M , Dumitrescu A , Refetoff S , Huynh T , Weiss RE |
| Ref : BMC Med Genet , 19 :69 , 2018 |
| Abstract : Watanabe_2018_BMC.Med.Genet_19_69 |
| ESTHER : Watanabe_2018_BMC.Med.Genet_19_69 |
| PubMedSearch : Watanabe_2018_BMC.Med.Genet_19_69 |
| PubMedID: 29720101 |
| Gene_locus related to this paper: human-TG |