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Atherosclerosis
Volume 170, Issue 1
, Pages
105-113
, September 2003
A novel LCAT mutation (Phe382→Val) in a kindred with familial LCAT deficiency and defective apolipoprotein B-100
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PII: S0021-9150(03)00241-7
doi: 10.1016/S0021-9150(03)00241-7
© 2003 Elsevier Ireland Ltd. All rights reserved.
« Previous
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Atherosclerosis
Volume 170, Issue 1
, Pages
105-113
, September 2003
