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Atherosclerosis
Volume 206, Issue 2
, Pages
346-348
, October 2009
Two novel frame shift mutations in lecithin:cholesterol acyltransferase (LCAT) gene associated with a familial LCAT deficiency phenotype
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PII: S0021-9150(09)00154-3
doi: 10.1016/j.atherosclerosis.2009.03.001
© 2009 Elsevier Ireland Ltd. All rights reserved.
« Previous
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Atherosclerosis
Volume 206, Issue 2
, Pages
346-348
, October 2009
