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5. Hereditary lecithin-cholesterol acyltransferase deficiency and Bloom syndrome in the same individual. Shojania AM; McAlpine PJ; Ray M Am J Med Genet; 1983 Mar; 14(3):479-85. PubMed ID: 6859101 [TBL] [Abstract][Full Text] [Related]
12. [Corneal opacity as the leading symptom of hereditary lecithin-cholesterol acyltransferase (LCAT) deficiency. Case report and a review of the literature]. Weidle EG; Lisch W Klin Monbl Augenheilkd; 1987 Mar; 190(3):182-7. PubMed ID: 3586537 [TBL] [Abstract][Full Text] [Related]
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20. A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia. Rial-Crestelo D; Santos-Recuero I; Julve J; Blanco-Vaca F; Torralba M J Clin Lipidol; 2017; 11(6):1475-1479.e3. PubMed ID: 28942093 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]