{"id":"W2157788198","doi":"10.1016/s0092-8674(01)00342-7","title":"Mutations in Kir2.1 Cause the Developmental and Episodic Electrical Phenotypes of Andersen's Syndrome","year":2001,"lang":"en","type":"article","venue":"Cell","topic":"Ion channel regulation and function","field":"Biochemistry, Genetics and Molecular Biology","cited_by":998,"is_retracted":false,"has_abstract":false,"ca_institutions":"London Health Sciences Centre","funders":"National Center for Research Resources; National Institute of Neurological Disorders and Stroke","keywords":"Biology; Missense mutation; Xenopus; Phenotype; Genetics; Periodic paralysis; Locus (genetics); Loss function; Mutation; Gene; Paralysis","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":0.01193098784674588,"score_gpt":0.2236300389203232,"score_spread":0.2116990510735773,"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."}}