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Autosomal recessive hypercholesterolemia in a Sicilian kindred harboring the 432insA mutation of the ARH gene.
Barbagallo, C M; Emmanuele, G; Cefalù, A B; Fiore, B; Noto, D; Mazzarino, M C; Pace, A; Brogna, A; Rizzo, M; Corsini, A; Notarbartolo, A; Travali, S; Averna, M R.
Affiliation
  • Barbagallo CM; Department of Internal Medicine, Istituto di Medicina Interna e Geriatria, Policlinico Paolo Giaccone, University of Palermo, Via del Vespro 141, 90127 Palermo, Italy.
Atherosclerosis ; 166(2): 395-400, 2003 Feb.
Article in En | MEDLINE | ID: mdl-12535754
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / Coronary Stenosis / Adaptor Proteins, Vesicular Transport / Adaptor Proteins, Signal Transducing / Genes, Recessive / Heterozygote / Hyperlipoproteinemia Type II Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Atherosclerosis Year: 2003 Document type: Article Affiliation country:
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: Point Mutation / Coronary Stenosis / Adaptor Proteins, Vesicular Transport / Adaptor Proteins, Signal Transducing / Genes, Recessive / Heterozygote / Hyperlipoproteinemia Type II Type of study: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male Country/Region as subject: Europa Language: En Journal: Atherosclerosis Year: 2003 Document type: Article Affiliation country: