Das hereditäre nicht-medulläres Schilddrüsenkarzinom 3 ist eine autosomal dominante Erkrankung, die durch Mutationen in der Chomosomenregion 2q21 ausgelöst wird.
1. |
Burgess JR et al. (1997) Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid. |
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Vriens MR et al. (2009) Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer. |
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McKay JD et al. (1999) At least three genes account for familial papillary thyroid carcinoma: TCO and MNG1 excluded as susceptibility loci from a large Tasmanian family. |
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McKay JD et al. (2001) Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21. |
5. |
OMIM.ORG article Omim 606240 |