(Q28586449)
Statements
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Point mutations in apolipoprotein A-I mimic the phenotype observed in patients with classical lecithin:cholesterol acyltransferase deficiency (English)
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Angeliki Chroni
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Adelina Duka
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Horng-Yuan Kan
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Tong Liu
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1 November 2005
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44
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43
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Identifiers
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