Role of miR-24 in Multiple Endocrine Neoplasia Type 1: A Potential Target for Molecular Therapy

Multiple endocrine neoplasia type 1 (MEN1) is a rare autosomal dominant inherited multiple cancer syndrome of neuroendocrine tissues. Tumors are caused by an inherited germinal heterozygote inactivating mutation of the MEN1 tumor suppressor gene, followed by a somatic loss of heterozygosity (LOH) of...

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Detalles Bibliográficos
Autores principales: Marini, Francesca, Brandi, Maria Luisa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Review
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306915/
https://www.ncbi.nlm.nih.gov/pubmed/34298972
http://dx.doi.org/10.3390/ijms22147352

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306915/
https://www.ncbi.nlm.nih.gov/pubmed/34298972
http://dx.doi.org/10.3390/ijms22147352

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