Evolution of Paget's disease of bone in adults inheritingSQSTM1mutations
Author:
Affiliation:
1. Department of Medicine; FMHS; University of Auckland; Auckland New Zealand
2. Department of Nuclear Medicine; Auckland City Hospital; Auckland New Zealand
Funder
Health Research Council of New Zealand
Publisher
Wiley
Subject
Endocrinology, Diabetes and Metabolism,Endocrinology
Reference18 articles.
1. Recurrent mutation of the gene encoding sequestosome 1 (SQSTM1/p62) in Paget disease of bone;Laurin;American Journal of Human Genetics,2002
2. Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease;Hocking;Human Molecular Genetics,2002
3. Novel UBA domain mutations of SQSTM1 in Paget's disease of bone: genotype phenotype correlation, functional analysis, and structural consequences;Hocking;Journal of Bone and Mineral Research,2004
4. Epidemiology of Paget's disease in Europe: the prevalence is decreasing;Poor;Journal of Bone and Mineral Research,2006
5. Paget's disease of bone - becoming a rarity?;Bastin;Rheumatology,2009
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