Author:
Kotani Tomio,Umeki Kazumi,Kawano Jun-ichi,Suganuma Tatsuo,Hishinuma Akira,Ieiri Tamio,Harada Shohei
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Reference34 articles.
1. Identification of a mutation in the coding sequence of the human thyroid peroxidase gene causing congenital goiter;Abramowicz;Journal of Clinical Investigation,1992
2. Novel mutations of the TPO gene in patients with permanent congenital hypothyroidism;Ambrugger;European Journal of Endocrinology,2001
3. Two decades of screening for congenital hypothyroidism in The Netherlands: TPO gene mutations in total iodide organification defects;Bakker;Journal of Clinical Endocrinology and Metabolism,2000
4. Maternal isodisomy for chromosome 2p causing severe congenital hypothyroidism;Bakker;Journal of Clinical Endocrinology and Metabolism,2001
5. A 20-basepair duplication in the human thyroid peroxidase gene resuls in a total iodide organification defect and congenital hypothyroidism;Bikker;Journal of Clinical Endocrinology and Metabolism,1994
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