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