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Mutations in TBL1X as a Novel Cause of Familial Central Hypothyroidism
Mutations in TBL1X as a Novel Cause of Familial Central Hypothyroidism
2016
Charlotte A Heinen
Monique Losekoot
Yu Sun
Peter Watson
Louise Fairall
Sjoerd D. Joustra
Nitash Zwaveling-Soonawala
Wilma Oostdijk
den Akker Erica van
Gijs W.E. Santen
Rijn Rick van
Wouter Dreschler
Olga V. Surovtseva
Nienke R. Biermasz
Raoul Hennekam
Jan Maarten Wit
John W. R. Schwabe
Anita Boelen
Eric Fliers
Trotsenburg Paul van
Keywords:
Endocrinology
Central hypothyroidism
TBL1X
Internal medicine
Medicine
Correction
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