A Rare Case of Heterozygous Gain of Function Thyrotropin Receptor Mutation Associated with Development of Thyroid Follicular Carcinoma

<div>Schematic representation of<i> TSHR</i> containing 10 exons (numbered 1-10 in red) with the introns represented by the horizontal line joining the exons. The grey region represents the untranslated region (UTR). The position of the variant at the position 1703 is shown in exon 10.</div>

Case Reports in Genetics

fig3

Figure 3

Figure 3: A Rare Case of Heterozygous Gain of Function Thyrotropin Receptor Mutation Associated with Development of Thyroid Follicular Carcinoma 