Association of Inherited Copy Number Variation in ADAM3A and ADAM5 Pseudogenes with Oropharynx Cancer Risk and Outcome

Inherited copy number variations (CNVs) can provide valuable information for cancer susceptibility and prognosis. However, their association with oropharynx squamous cell carcinoma (OPSCC) is still poorly studied. Using microarrays analysis, we identified three inherited CNVs associated with OPSCC r...

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Detalles Bibliográficos
Autores principales: Carron, Juliana, Torricelli, Caroline, Silva, Janet Keller, Liu, Yichuan, Pellegrino, Renata, Lima, Carmen Silvia Passos, Lourenço, Gustavo Jacob
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778539/
https://www.ncbi.nlm.nih.gov/pubmed/36553675
http://dx.doi.org/10.3390/genes13122408

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9778539/
https://www.ncbi.nlm.nih.gov/pubmed/36553675
http://dx.doi.org/10.3390/genes13122408

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