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.
申请公布号
EP1414960(A2)
申请公布日期
2004.05.06
申请号
EP20020748529
申请日期
2002.07.30
申请人
G.R.M.O. (GROUPE DE RECHERCHE EN MALADIES OSSEUSES) INC.
