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