A mutation in p62 protein (p. R321C), associated to Paget’s disease of bone, causes a blockade of autophagy and an activation of NF-kB pathway

Autores INICO

Javier del Pino Montes

Otros Autores

Nerea Gestoso Uzal, Rogelio González Sarmiento

Referencia

Usategui-Martín, R., Gestoso-Uzal, N., Calero-Paniagua, I., De Pereda, J. M., del Pino-Montes, J., & González-Sarmiento, R. (2020). A mutation in p62 protein (p. R321C), associated to Paget’s disease of bone, causes a blockade of autophagy and an activation of NF-kB pathway. Bone, 133. https://doi.org/10.1016/J.BONE.2020.115265

Fecha publicación (año)
DOI

10.1016/J.BONE.2020.115265