A common thyroid peroxidase gene mutation (G319R) in Turkish patients with congenital hypothyroidism could be due to a founder effect.


Baş V. N., Aycan Z., Cangul H., Kendall M., Ağladıoğlu S., Çetinkaya S., ...More

Journal of pediatric endocrinology & metabolism : JPEM, vol.27, pp.383-7, 2014 (SCI-Expanded) identifier identifier identifier