| 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 |
| Gene_locus related to this paper: human-TG |
Watanabe Y, Sharwood E, Goodwin B, Creech MK, Hassan HY, Netea MG, Jaeger M, Dumitrescu A, Refetoff S, Huynh T, Weiss RE (2018)
A novel mutation in the TG gene (G2322S) causing congenital hypothyroidism in a Sudanese family: a case report
BMC Med Genet
19 :69
Watanabe Y, Sharwood E, Goodwin B, Creech MK, Hassan HY, Netea MG, Jaeger M, Dumitrescu A, Refetoff S, Huynh T, Weiss RE (2018)
BMC Med Genet
19 :69