{"id":"W2116807721","doi":"10.1093/hmg/11.22.2735","title":"Domain-specific mutations in sequestosome 1 (SQSTM1) cause familial and sporadic Paget's disease","year":2002,"lang":"en","type":"article","venue":"Human Molecular Genetics","topic":"Cancer-related Molecular Pathways","field":"Medicine","cited_by":345,"is_retracted":false,"has_abstract":true,"ca_institutions":"","funders":"Medical Research Council; Vlaamse regering; Fonds Wetenschappelijk Onderzoek; Wellcome Trust","keywords":"Sequestosome 1; Genetics; Paget's disease of bone; Biology; Exon; Mutation; Protein Data Bank (RCSB PDB); Locus (genetics); Gene; Missense mutation; Disease; Medicine; Pathology; Immunoglobulin light chain","routes":{"ca_aff":false,"ca_fund":false,"ca_venue":false,"about_ca":true,"invisible_to_affiliation_only":true},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.03052048545231557,"score_gpt":0.259077294362346,"score_spread":0.2285568089100304,"validation_status":"score_only:v0-immature-baseline","note":"Baseline scores from an immature model (maturity gate not passed). Scores rank; they never assert a category."}}