FOXE1 polymorphism rs965513 predisposes to thyroid cancer in a European cohort

OBJECTIVE: FOXE1 is an intronless gene on chromosome 9 which plays a significant role in thyroid morphogenesis. Mutations in FOXE1 are associated with thyroid phenotypes including congenital hypothyroidism, thyroid dysgenesis and thyroid cancer. This study aims to investigate the frequency and impac...

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Detalles Bibliográficos
Autores principales: Owens, Patrick W, McVeigh, Terri Patricia, Miller, Nicola, Guerin, Carole, Sebag, Frederic, Quill, Denis, Bell, Marcia, Kerin, Michael J, Lowery, Aoife J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2021
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265543/
https://www.ncbi.nlm.nih.gov/pubmed/37435181
http://dx.doi.org/10.1530/EO-21-0003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10265543/
https://www.ncbi.nlm.nih.gov/pubmed/37435181
http://dx.doi.org/10.1530/EO-21-0003

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