Analysis of Newly Identified and Rare Synonymous Genetic Variants in the RET Gene in Patients with Medullary Thyroid Carcinoma in Polish Population.

Endocr Pathol · 2017 · PMC5552825 · PMID 28647780

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extremely significantno p-value reported

Identification of these rare changes in the context of specific symptoms of the disease is extremely significant for a better understanding of the role they potentially play in the RET receptor function.

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