{"id":"W4206477217","doi":"10.1038/nrdp.2017.52","title":"Osteogenesis imperfecta","year":2017,"lang":"en","type":"review","venue":"Nature Reviews Disease Primers","topic":"Connective tissue disorders research","field":"Biochemistry, Genetics and Molecular Biology","cited_by":758,"is_retracted":false,"has_abstract":false,"ca_institutions":"Shriners Hospitals for Children - Canada; Montreal Children's Hospital; McGill University","funders":"Eunice Kennedy Shriver National Institute of Child Health and Human Development; National Institute of Arthritis and Musculoskeletal and Skin Diseases","keywords":"Osteogenesis imperfecta; Dentinogenesis imperfecta; Medicine; Locus heterogeneity; Osteochondrodysplasia; Bone disease; Pathology; Bioinformatics; Genetic heterogeneity; Biology; Genetics; Phenotype; Gene; Osteoporosis","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":null,"machine_scores":{"provisional":true,"baseline":true,"maturity_gate_passed":false,"score_opus":0.1033639602209408,"score_gpt":0.4708384140598942,"score_spread":0.3674744538389534,"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."}}