Modifier Role of Common RET Variants in Sporadic Medullary Thyroid Carcinoma

Background: Although the disease-causing effect of pathogenic variants in the gene RET has been unambiguously identified, there is a lack of consensus regarding the possible impact of common variants in this gene. Our study aimed to test whether variants in exons 10, 11, and 13–16 that are commonly...

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Detalles Bibliográficos
Autores principales: Skalniak, Anna, Trofimiuk-Müldner, Małgorzata, Przybylik-Mazurek, Elwira, Hubalewska-Dydejczyk, Alicja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8583971/
https://www.ncbi.nlm.nih.gov/pubmed/34769224
http://dx.doi.org/10.3390/ijms222111794

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8583971/
https://www.ncbi.nlm.nih.gov/pubmed/34769224
http://dx.doi.org/10.3390/ijms222111794

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