Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease

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 journalArticlepeer-review

293 Citations (Scopus)

Fingerprint

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.

Medicine & Life Sciences