A mutation in p62 protein (p. R321C), associated to Paget's...

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

Usategui-Martín, Ricardo, Gestoso-Uzal, Nerea, Calero-Paniagua, Ismael, De Pereda, José María, del Pino-Montes, Javier, González-Sarmiento, Rogelio
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Volume:
133
Journal:
Bone
DOI:
10.1016/j.bone.2020.115265
Date:
April, 2020
File:
PDF, 3.52 MB
2020
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