Associated Papers
Screening of frequent variants associated with congenital hypothyroidism: a comparison with next generation sequencing.
Watanabe D et al.
Endocrine Journal, 2021
Variant of TSHR is Not a Frequent Cause of Congenital Hypothyroidism in Chinese Han Patients.
Xue P et al.
International Journal of General Medicine, 2021
A novel c.1391_1428delinsT mutation in TSHR as a cause of familial congenital hypothyroidism with delayed onset.
Watanabe D et al.
Pediatrics and Neonatology, 2020
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