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- W2031141892 abstract "Acta Medica ScandinavicaVolume 210, Issue 1-6 p. 1-2 Free Access Genetic Heterogeneity in Familial Lecithin:Cholesterol Acyltransferase (LCAT) Deficiency P. Teisberg, P. Teisberg Medical Department, Rikshospitalet, University of Oslo, Oslo, NorwaySearch for more papers by this authorE. Gjone, E. Gjone Medical Department, Rikshospitalet, University of Oslo, Oslo, NorwaySearch for more papers by this author P. Teisberg, P. Teisberg Medical Department, Rikshospitalet, University of Oslo, Oslo, NorwaySearch for more papers by this authorE. Gjone, E. Gjone Medical Department, Rikshospitalet, University of Oslo, Oslo, NorwaySearch for more papers by this author First published: January/December 1981 https://doi.org/10.1111/j.0954-6820.1981.tb09766.xCitations: 15AboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1 Albers, J. J., Adolphson, J. L. & Chen, C.-H.: Radioimmunoassay of human plasma lecithin-cholesterol acyltransferase. J Clin Invest 67: 141, 1981. 2 Albers, J. J. & Utermann, G.: Genetic control of lecithin-cholesterol acyltransferase: Measurement of LCAT mass in a large kindred with LCAT deficiency. Am J Hum Genet. In press 1981. 3 Gjone, E.: Familial LCAT deficiency. Acta Med Scand 194: 353, 1973. 4 Gjone, E.: Familial lecithin:cholesterol acyltransferase deficiency—a new metabolic disease with renal involvement. Adv Nephrol 10: 167, 1981. 5 Gjone, E., Blomhoff, J. P., Holme, R. et al.: Familial lecithin:cholesterol acyltransferase deficiency. Report of a fourth family from Northwestern Norway. Acta Med Scand 210: 3, 1981. 6 Gjone, E. & Norum, K. R.: Familial serum cholesterol ester deficiency. Clinical study of a patient with a new syndrome. Acta Med Scand 183: 107, 1968. 7 Gjone, E., Skarbøvik, A. J., Blomhoff, J. P. & Teisberg, P.: Familial lecithin:cholesterol acyltransferase deficiency. Report of a third Norwegian family with two afflicted members. Scand J Clin Lab Invest (Suppl) 137: 101, 1974. 8 Hamnstrøm, B., Gjone, E. & Norum, K. R.: Familial plasma lecithin:cholesterol acyltransferase deficiency. Br Med J 2: 283, 1969. 9 Iwamoto, A., Naito, C., Teramoto, T. et al.: Familial lecithin:cholesterol acyltransferase deficiency complicated with unconjugated hyperbilirubinemia and peripheral neuropathy. The first reported case in the Far East. Acta Med Scand 204: 219, 1978. 10 Norum, K. R. & Gjone, E.: Familial plasma lecithin:cholesterol acyltransferase deficiency. Biochemical study of a new inborn error of metabolism. Scand J Clin Lab Invest 20: 231, 1967. 11 Teisberg, P., Gjone, E. & Olaisen, B.: Genetics of lecithin:cholesterol acyltransferase deficiency. Ann Hum Genet 38: 327, 1975. 12 Utermann, G., Menzel, H. J., Dieber, P., Langer, K. H. & Fiorelli, G.: Lecithin-cholesterol-acyltransfer-ase deficiency: Autosomal recessive transmission in a large kindred. Clin Genet. In press 1981. Citing Literature Volume210, Issue1-6January/December 1981Pages 1-2 ReferencesRelatedInformation" @default.
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- W2031141892 title "Genetic Heterogeneity in Familial Lecithin:Cholesterol Acyltransferase (LCAT) Deficiency" @default.
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