Mutational and bioinformatics analysis of the NKX2.1 gene in a cohort of Iranian pediatric patients with congenital hypothyroidism (CH).
| Autor: | Heidari, Mohammad Mehdi, Madani Manshadi, Seyed Ali, Eshghi, Ahmad Reza, Talebi, Fatemeh, Khatami, Mehri, Bragança, José, Ordooei, Mahtab, Chamani, Reyhane, Ghasemi, Farzaneh |
|---|---|
| Zdroj: | Physiology International; Jun2022, Vol. 109 Issue 2, p261-277, 17p |
| Databáze: | Complementary Index |
| Externí odkaz: |
|