Sporadic nonautoimmune neonatal hyperthyroidism due to A623V germline mutation in the thyrotropin receptor gene.


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Aycan Z., Ağladıoğlu S., Ceylaner S., Cetinkaya S., Baş V. N., Kendirici H.

Journal of clinical research in pediatric endocrinology, vol.2, pp.168-72, 2010 (SCI-Expanded) identifier identifier