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Title : Homozygous lecithin:cholesterol acyltransferase (LCAT) deficiency due to a new loss of function mutation and review of the literature - Roshan_2011_J.Clin.Lipidol_5_493 |
Author(s) : Roshan B , Ganda OP , Desilva R , Ganim RB , Ward E , Haessler SD , Polisecki EY , Asztalos BF , Schaefer EJ |
Ref : J Clin Lipidol , 5 :493 , 2011 |
Abstract : Roshan_2011_J.Clin.Lipidol_5_493 |
ESTHER : Roshan_2011_J.Clin.Lipidol_5_493 |
PubMedSearch : Roshan_2011_J.Clin.Lipidol_5_493 |
PubMedID: 22108153 |
Gene_locus related to this paper: human-LCAT |