Associated Papers
Functional mutations in the thyroid-stimulating hormone receptor in natural stickleback populations at sites identical to human disease-causing mutations.
Kitano J et al.
Bmc Ecology and Evolution, 2025
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
Targeted next-generation sequencing of thirteen causative genes in Chinese patients with congenital hypothyroidism.
Long W et al.
Endocrine Journal, 2018
Newborn Screening and Molecular Profile of Congenital Hypothyroidism in a Chinese Population.
Yu B et al.
Frontiers in Genetics, 2018
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