| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 8478817 | Molecular and Cellular Probes | 2009 | 6 Pages |
Abstract
In conclusion, we report thirteen patients with RTH caused by heterozygous mutations of the THRB gene. Seven of the identified mutations correspond to novel substitutions.
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Authors
Carina M. Rivolta, MarÃa C. Olcese, Fiorella S. Belforte, Ana Chiesa, Laura Gruñeiro-Papendieck, Sonia Iorcansky, Viviana Herzovich, Fernando Cassorla, Alicia Gauna, Rogelio Gonzalez-Sarmiento, Héctor M. Targovnik,