{"id":"W2624801309","doi":"10.1016/j.jacl.2017.06.005","title":"A case of hypocholesterolemia and steatosis in a carrier of a PCSK9 loss-of-function mutation and polymorphisms predisposing to nonalcoholic fatty liver disease","year":2017,"lang":"en","type":"article","venue":"Journal of clinical lipidology","topic":"Lipoproteins and Cardiovascular Health","field":"Medicine","cited_by":11,"is_retracted":false,"has_abstract":false,"ca_institutions":"Université de Montréal; Montreal Clinical Research Institute","funders":"","keywords":"Medicine; Steatosis; Hypocholesterolemia; Nonalcoholic fatty liver disease; Fatty liver; Internal medicine; Loss function; Disease; Mutation; Gastroenterology; Genetics; Gene; Cholesterol; Phenotype; Biology","routes":{"ca_aff":true,"ca_fund":false,"ca_venue":false,"about_ca":false,"invisible_to_affiliation_only":false},"retraction":null,"screen":{"n_in":0,"stratum":"aff_core","weight":5595.2375,"opus":{"tier":"OUT","genre":"empirical","about_ca":false,"confidence":"high","reason":"Clinical case report of a PCSK9 mutation carrier."},"gpt":{"tier":"OUT","genre":"empirical","about_ca":false,"confidence":"high","reason":"This reports a clinical case involving a genetic mutation and liver disease, not research itself."},"grok":{"tier":"OUT","genre":"empirical","about_ca":false,"confidence":"medium","reason":"Clinical genetics case of PCSK9 mutation and steatosis; title-domain clear despite empty abstract."}}}