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      Two compound heterozygous mutations (c.215delA/c.2422T?C and c.387delC/c.1159G?A) in the thyroid peroxidase gene responsible for congenital goitre and iodide organification defect

      Clinical Endocrinology

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          Journal
          10.1111/j.1365-2265.2007.02869.x

          Endocrinology & Diabetes,Medicine
          Endocrinology & Diabetes, Medicine

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