Clinical Study

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

Figure 2

Family pedigree of the index patient. A family pedigree of two sisters with congenital hypothyroidism and multinodular goiter. The proband is indicated by an arrow. N/A: data are not available; TSH: thyrotropin; TT4: total thyroxine; FT4: free thyroxine; Tg, thyroglobulin.
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