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Dive into the research topics of 'Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease'. Together they form a unique fingerprint.- Sort by
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Lynne Hocking, Gavin Lucas, Anna Daroszewska, J. Mangion, M. Olavesen, T. Cundy, G. C. Nicholson, L. Ward, S. T. Bennett, W. Wuyts, W. Van Hul, S Ralston
Research output: Contribution to journal › Article › peer-review