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Dive into the research topics of 'Structural and functional studies of mutations affecting the UBA domain of SQSTM1 (p62) which cause Paget's disease of bone'. Together they form a unique fingerprint.- Sort by
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R. Layfield, B. Ciani, S Ralston, Lynne Hocking, P. W. Sheppard, MS. Searle, J. R. Cavey
Research output: Contribution to journal › Article › peer-review