High prevalence of a novel mutation (2268 insT) of the thyroid peroxidase gene in Taiwanese patients with total iodide organification defect, and evidence for a founder effect.

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🔗 View Article (PMID 12213873)

Published in J Clin Endocrinol Metab on September 01, 2002

Authors

Dau-Ming Niu1, Betau Hwang, Yum-Kung Chu, Chun-Ju Liao, Pei-Ling Wang, Ching-Yuang Lin

Author Affiliations

1: Department of Pediatrics, Veterans General Hospital-Taipei, Taiwan.

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