Associated Papers
Central Hypothyroidism Due to a TRHR Mutation Causing Impaired Ligand Affinity and Transactivation of Gq.
García M et al.
The Journal of Clinical Endocrinology and Metabolism, 2017
The multiple genetic causes of central hypothyroidism.
Persani L et al.
Best Practice & Research. Clinical Endocrinology & Metabolism, 2017
A Novel Thyrotropin-Releasing Hormone Receptor Missense Mutation (P81R) in Central Congenital Hypothyroidism.
Koulouri O et al.
The Journal of Clinical Endocrinology and Metabolism, 2016
Recent advances in central congenital hypothyroidism.
Schoenmakers N et al.
The Journal of Endocrinology, 2015
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