A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the <i>Thyroid peroxidase</i> Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter

<table>Homology model of the wild type human TPO using sheep lactoperoxidase as a template (PDB_2IKC). The positions of the annotated functional site referred from UniProt database (reference number: P07202). The arrow indicates the positions of the mutated residue (p.Val501Gly).</table>

International Journal of Endocrinology

fig4

Figure 4

Figure 4: A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the <i>Thyroid peroxidase</i> Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter 

Figure 4 | A Novel, Homozygous c.1502T>G (p.Val501Gly) Mutation in the Thyroid peroxidase Gene in Malaysian Sisters with Congenital Hypothyroidism and Multinodular Goiter 