Laboratory for Molecular Diagnostics
Center for Nephrology and Metabolic Disorders
Familial follicular thyroid carcinoma is an autosomal dominant disorder seen with mutations in the MINPP1 gene.
| 1. |
He H et al. (2013) SRGAP1 is a candidate gene for papillary thyroid carcinoma susceptibility. 
|
| 2. |
Vriens MR et al. (2009) Clinical features and genetic predisposition to hereditary nonmedullary thyroid cancer.
|
| 3. |
Bonora E et al. (2010) Genetic Predisposition to Familial Nonmedullary Thyroid Cancer: An Update of Molecular Findings and State-of-the-Art Studies.
|
| 4. |
OMIM.ORG article Omim 188470
|
 |
Copyright © 2005-2025 by Center for Nephrology and Metabolic Disorders, Dr. Mato Nagel, MD Albert-Schweitzer-Ring 32, D-02943 Weißwasser, Germany, Tel.: +49-3576-287922, Fax: +49-3576-287944 Sitemap | Webmail | Disclaimer | Privacy Issues | Website Credits |
