Mutations in the atypical protein kinase C-interacting protein p62/sequestosome 1 (p62/SQSTM1) causing Paget disease of bone are described. Methods of detecting and treating Paget disease of bone are also disclosed.

 
Web www.patentalert.com

< Prodrugs of 2,4-pyrimidinediamine compounds and their uses

> FIAT nucleic acids and proteins and uses thereof

~ 00492