{"id":"W2072981065","doi":"10.1038/nature10353","title":"Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia","year":2011,"lang":"de","type":"article","venue":"Nature","topic":"Amyotrophic Lateral Sclerosis Research","field":"Medicine","cited_by":1171,"is_retracted":false,"has_abstract":false,"ca_institutions":"Ottawa Hospital; Children's Hospital of Eastern Ontario; University of Ottawa","funders":"National Institute on Aging; National Institute of Neurological Disorders and Stroke; Robert H. Lurie Comprehensive Cancer Center; National Cancer Institute; MND Scotland; National Institutes of Health; Blazeman Foundation for ALS; Northwestern University","keywords":"Amyotrophic lateral sclerosis; TARDBP; Neurodegeneration; Frontotemporal dementia; Dementia; Frontotemporal lobar degeneration; Biology; Mutation; SOD1; C9orf72; Genetics; Pathology; Medicine; Gene; Disease","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":0.02841822338458216,"score_gpt":0.3115295560203403,"score_spread":0.2831113326357582,"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."}}