| Title : Compound heterozygous DUOX2 gene mutations (c.2335-1G>C\/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis - Belforte_2016_Mol.Cell.Endocrinol_419_172 |
| Author(s) : Belforte FS , Citterio CE , Testa G , Olcese MC , Sobrero G , Miras MB , Targovnik HM , Rivolta CM |
| Ref : Mol Cell Endocrinol , 419 :172 , 2016 |
| Abstract : Belforte_2016_Mol.Cell.Endocrinol_419_172 |
| ESTHER : Belforte_2016_Mol.Cell.Endocrinol_419_172 |
| PubMedSearch : Belforte_2016_Mol.Cell.Endocrinol_419_172 |
| PubMedID: 26506010 |
Belforte FS, Citterio CE, Testa G, Olcese MC, Sobrero G, Miras MB, Targovnik HM, Rivolta CM (2016)
Compound heterozygous DUOX2 gene mutations (c.2335-1G>C\/c.3264_3267delCAGC) associated with congenital hypothyroidism. Characterization of complex cryptic splice sites by minigene analysis
Mol Cell Endocrinol
419 :172
Belforte FS, Citterio CE, Testa G, Olcese MC, Sobrero G, Miras MB, Targovnik HM, Rivolta CM (2016)
Mol Cell Endocrinol
419 :172