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