| Title : The p.A2215D thyroglobulin gene mutation leads to deficient synthesis and secretion of the mutated protein and congenital hypothyroidism with wide phenotype variation - Pardo_2009_J.Clin.Endocrinol.Metab_94_2938 |
| Author(s) : Pardo V , Vono-Toniolo J , Rubio IG , Knobel M , Possato RF , Targovnik HM , Kopp P , Medeiros-Neto G |
| Ref : J Clinical Endocrinology Metab , 94 :2938 , 2009 |
| Abstract : |
| PubMedSearch : Pardo_2009_J.Clin.Endocrinol.Metab_94_2938 |
| PubMedID: 19509106 |
| Gene_locus related to this paper: human-TG |
| Title : Mutations of the thyroglobulin gene and its relevance to thyroid disorders - Rubio_2009_Curr.Opin.Endocrinol.Diabetes.Obes_16_373 |
| Author(s) : Rubio IG , Medeiros-Neto G |
| Ref : Curr Opin Endocrinol Diabetes Obes , 16 :373 , 2009 |
| Abstract : |
| PubMedSearch : Rubio_2009_Curr.Opin.Endocrinol.Diabetes.Obes_16_373 |
| PubMedID: 19633549 |
| Title : A molecular analysis and long-term follow-up of two siblings with severe congenital hypothyroidism carrying the IVS30+1G>T intronic thyroglobulin mutation - Rubio_2008_Arq.Bras.Endocrinol.Metabol_52_1337 |
| Author(s) : Rubio IG , Galrao AL , Pardo V , Knobel M , Possato RF , Camargo RR , Ferreira MA , Kanamura CT , Gomes SA , Medeiros-Neto G |
| Ref : Arq Bras Endocrinol Metabol , 52 :1337 , 2008 |
| Abstract : |
| PubMedSearch : Rubio_2008_Arq.Bras.Endocrinol.Metabol_52_1337 |
| PubMedID: 19169491 |
| Title : Phenotypic variation among four family members with congenital hypothyroidism caused by two distinct thyroglobulin gene mutations - Pardo_2008_Thyroid_18_783 |
| Author(s) : Pardo V , Rubio IG , Knobel M , Aguiar-Oliveira MH , Santos MM , Gomes SA , Oliveira CR , Targovnik HM , Medeiros-Neto G |
| Ref : Thyroid , 18 :783 , 2008 |
| Abstract : |
| PubMedSearch : Pardo_2008_Thyroid_18_783 |
| PubMedID: 18631008 |
| Gene_locus related to this paper: human-TG |