Author:
Simm Diemud,Pfarr Nicole,Pohlenz Joachim,Prawitt Dirk,Dörr Helmuth G.
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Reference30 articles.
1. High prevalence of thyroid peroxidase gene mutations in patients with thyroid dyshormonogenesis;Avbelj;Eur J Endocrinol,2007
2. Novel mutations of the thyroid peroxidase gene in patients with permanent congenital hypothyroidism;Ambrugger;Eur J Endocrinol,2001
3. Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects (an update);Bakker;J Clin Endocrinol Metab,2000
4. Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects;Bikker;J Clin Endocrinol Metab,1997
5. A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism;Bikker;J Clin Endocrinol Metab,1994
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