Der Typ 3 der Neigung zu autoimmunbedingten Schilddrüsenerkrankungen wird durch Polymorphismen im ZFAT- und TG-Gen verursacht.
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Ban Y et al. (2003) Amino acid substitutions in the thyroglobulin gene are associated with susceptibility to human and murine autoimmune thyroid disease. ![]() |
2. |
Collins JE et al. (2004) Common allelic variants of exons 10, 12, and 33 of the thyroglobulin gene are not associated with autoimmune thyroid disease in the United Kingdom. ![]() |
3. |
Shirasawa S et al. (2004) SNPs in the promoter of a B cell-specific antisense transcript, SAS-ZFAT, determine susceptibility to autoimmune thyroid disease. ![]() |
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Tomer Y et al. (1999) Mapping the major susceptibility loci for familial Graves' and Hashimoto's diseases: evidence for genetic heterogeneity and gene interactions. ![]() |
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Tomer Y et al. (2003) Common and unique susceptibility loci in Graves and Hashimoto diseases: results of whole-genome screening in a data set of 102 multiplex families. ![]() |
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Collins JE et al. (2003) Association of a rare thyroglobulin gene microsatellite variant with autoimmune thyroid disease. ![]() |
8. |
Tomer Y et al. (2002) Thyroglobulin is a thyroid specific gene for the familial autoimmune thyroid diseases. ![]() |
9. |
OMIM.ORG article Omim 608175![]() |