Analysis of the genetic variability of the 1st (CCC/ACC, P52T) and the 10th exons (bp 1012-1704) of the TSH receptor gene in Graves’ disease-Reference-Cited by-同舟云学术

Analysis of the genetic variability of the 1st (CCC/ACC, P52T) and the 10th exons (bp 1012-1704) of the TSH receptor gene in Graves’ disease

Published:2000-02 Issue:1 Volume:27 Page:17-23
ISSN:0960-7420
Container-title:European Journal of Immunogenetics
language:en
Short-container-title:

Author:

Kaczur Viktória,Takács Mária,Szalai Csaba,Falus András,Nagy Zsuzsa,Berencsi György,Balázs Csaba

Publisher

Wiley

Subject

Genetics,Immunology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1046/j.1365-2370.2000.00187.x/fullpdf

Reference50 articles.

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3. Tumor necrosis factor beta gene polymorphisms in Graves’ disease;Badenhoop;Journal of Clinical Endocrinology and Metabolism,1992

4. A genomic point mutation in the extracellular domain of the thyrotropin receptor in patients with Graves’ ophthalmopathy;Bahn;Journal of Clinical Endocrinology and Metabolism,1994

5. Serum soluble CD8 concentration is an indicator of disease activity in patients with Graves’ disease;Balázs;Thyroid,1994

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