{"id":"W1986126870","doi":"10.1002/1098-1004(2001)17:1<42::aid-humu5>3.0.co;2-k","title":"Prevalence of mutations causing retinitis pigmentosa and other inherited retinopathies","year":2000,"lang":"en","type":"article","venue":"Human Mutation","topic":"Retinal Development and Disorders","field":"Biochemistry, Genetics and Molecular Biology","cited_by":334,"is_retracted":false,"has_abstract":true,"ca_institutions":"","funders":"National Eye Institute","keywords":"Retinitis pigmentosa; Biology; Genetics; Peripherin; Rhodopsin; Mutation; Proband; Stargardt disease; ABCA4; Hereditary Diseases; Gene; Retinal; Phenotype","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":0.01422507017518397,"score_gpt":0.2632163429203478,"score_spread":0.2489912727451639,"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."}}