A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect-Reference-Cited by-同舟云学术

A novel mutation in the TPO gene in goitrous hypothyroid patients with iodide organification defect

Published:1999-08 Issue:2 Volume:51 Page:165-172
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Santos Cecilia L. S.,Bikker Hennie,Rego Katia G. M.,Nascimento Antonio C.,Tambascia Marcos,De Vijlder Jan J. M.,Medeiros-Neto Geraldo

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2265.1999.00746.x/fullpdf

Reference30 articles.

1. Identification of a mutation in the coding sequence of the human peroxidase gene causing congenital goitre;Abramowicz;Journal of Clinical Investigation,1992

2. Prediction of domain organization and secondary structure of thyroid peroxidase, a human autoantigen involved in destructive thyroiditis;Banga;FEBS Letters,1990

3. Molecular analysis of mutated thyroid peroxidase detected in patients with total iodide organification defects;Bikker;The Journal of Clinical Endocrinology and Metabolism,1997

4. A 20-basepair duplication in the human thyroid peroxidase gene results in a total iodide organification defect and congenital hypothyroidism;Bikker;The Journal of Clinical Endocrinology and Metabolism,1994

5. Thyroid Peroxidase (TPO) cDNA detects a VNTR polymorphism and reveals that the TPO gene is ≤140kb;Bikker;Annales d'Endocrinologie,1989

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