Prevalence of Selected Single-Nucleotide Variants in Patients with Neuroendocrine Tumors—Potential Clinical Relevance

Introduction: The genetic basis of neuroendocrine tumors (NETs), whose incidence is continuously increasing, is still not fully defined. The majority of NETs are sporadic, and only a small percentage occur as part of hereditary genetic syndromes. However, the associations of multiple genetic variant...

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Detalles Bibliográficos
Autores principales: Kurzyńska, Anna, Pach, Dorota, Skalniak, Anna Elżbieta, Stefańska, Agnieszka, Opalińska, Marta, Przybylik-Mazurek, Elwira, Hubalewska-Dydejczyk, Alicja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573749/
https://www.ncbi.nlm.nih.gov/pubmed/36233401
http://dx.doi.org/10.3390/jcm11195536

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9573749/
https://www.ncbi.nlm.nih.gov/pubmed/36233401
http://dx.doi.org/10.3390/jcm11195536

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