The modifier role of RET-G691S polymorphism in hereditary medullary thyroid carcinoma: functional characterization and expression/penetrance studies

BACKGROUND: Hereditary medullary thyroid carcinoma (MTC) is caused by germ-line gain of function mutations in the RET proto-oncogene, and a phenotypic variability among carriers of the same mutation has been reported. We recently observed this phenomenon in a large familial MTC (FMTC) family carryin...

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Veröffentlicht in:Orphanet J Rare Dis
Hauptverfasser: Colombo, Carla, Minna, Emanuela, Rizzetti, Maria Grazia, Romeo, Paola, Lecis, Daniele, Persani, Luca, Mondellini, Piera, Pierotti, Marco A, Greco, Angela, Fugazzola, Laura, Borrello, Maria Grazia
Format: Artigo
Sprache:Inglês
Veröffentlicht: BioMed Central 2015
Schlagworte:
Research
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC4373282/
https://ncbi.nlm.nih.gov/pubmed/25887804
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13023-015-0231-z
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