Founder Effect in Different European Countries for the Recurrent P392L SQSTM1 Mutation in Paget’s Disease of Bone

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Evaluation of the Role of the SQSTM1 Gene in Sporadic Belgian Patients with Paget’s Disease

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Identification and Molecular Characterization of a Novel Splice-Site Mutation ( G1205C ) in the SQSTM1 Gene Causing Paget’s Disease of Bone in an Extended American Family

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1st European Conference on Paget’s Disease of Bone

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Paget’s Disease of Bone in New Zealand: Continued Decline in Disease Severity

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