Autor: Yinbing Zhu
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Case report: co-inheritance of familial lecithin-cholesterol acyltransferase deficiency and α0-Thalassemia
BackgroundFamilial lecithin-cholesterol acyltransferase (LCAT) deficiency and α0-thalassemia are rare autosomal recessive disorders. Although both disease-causing genes reside on chromosome 16, their physical distance typically results in independent i…