Nicht-medulläres Schilddrüsenkarzinom 3
Das hereditäre nicht-medulläres Schilddrüsenkarzinom 3 ist eine autosomal dominante Erkrankung, die durch Mutationen in der Chomosomenregion 2q21 ausgelöst wird.
Gliederung
Referenzen:
| 1. |
Burgess JR et. al. (1997) Two families with an autosomal dominant inheritance pattern for papillary carcinoma of the thyroid. [^] |
| 2. |
Vriens MR et. al. (2009) Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer. [^] |
| 3. |
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. [^] |
| 4. |
McKay JD et. al. (2001) Localization of a susceptibility gene for familial nonmedullary thyroid carcinoma to chromosome 2q21. [^] |
