Characterization of a novel loss‐of‐function mutation of PAX8 associated with congenital hypothyroidism
- DOI
- 10.1111/j.1365-2265.2010.03851.x
- Published
- 2010-11-16
- Container
- Clinical Endocrinology
- Publisher
- Wiley
- Open access
- unknown
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Cite this work
BibTeX
@article{allodium:10.1111/j.1365-2265.2010.03851.x,
title = {Characterization of a novel loss‐of‐function mutation of PAX8 associated with congenital hypothyroidism},
author = {Tina Di Palma and Emilia Zampella and Maria Grazia Filippone and Paolo Emidio Macchia and Carrie Ris‐Stalpers and Monique De Vroede and Mariastella Zannini},
year = {2010},
journal = {Clinical Endocrinology},
doi = {10.1111/j.1365-2265.2010.03851.x},
url = {https://doi.org/10.1111/j.1365-2265.2010.03851.x}
}RIS
TY - JOUR TI - Characterization of a novel loss‐of‐function mutation of PAX8 associated with congenital hypothyroidism AU - Tina Di Palma AU - Emilia Zampella AU - Maria Grazia Filippone AU - Paolo Emidio Macchia AU - Carrie Ris‐Stalpers AU - Monique De Vroede AU - Mariastella Zannini PY - 2010 JO - Clinical Endocrinology DO - 10.1111/j.1365-2265.2010.03851.x UR - https://doi.org/10.1111/j.1365-2265.2010.03851.x ER -
APA
Palma, T. D., Zampella, E., Filippone, M. G., Macchia, P. E., Ris‐Stalpers, C., Vroede, M. D., & Zannini, M. (2010). Characterization of a novel loss‐of‐function mutation of PAX8 associated with congenital hypothyroidism. Clinical Endocrinology. https://doi.org/10.1111/j.1365-2265.2010.03851.x
Source records
- crossref · retrieved 2026-09-26T15:00:34.837Z