The clinical and molecular characterization of patients with dyshormonogenic congenital hypothyroidism reveals specific diagnostic clues for DUOX2 defects.
| Image |  |
|---|---|
| Description | scientific article published in January 2013 |
| Author/s |
author: Giovanna Weber Luca Persani Valentina Cirello Nadia Schoenmakers |
| Publication date | January 1, 2013 |
| Language | English |
| Country of origin | |
| Wikipedia link | |
| Copyright status | |
| Missing/wrong data? | Edit Wikidata item |