| Title : A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia - Rial-Crestelo_2017_J.Clin.Lipidol_11_1475 |
| Author(s) : Rial-Crestelo D , Santos-Recuero I , Julve J , Blanco-Vaca F , Torralba M |
| Ref : J Clin Lipidol , 11 :1475 , 2017 |
| Abstract : Rial-Crestelo_2017_J.Clin.Lipidol_11_1475 |
| ESTHER : Rial-Crestelo_2017_J.Clin.Lipidol_11_1475 |
| PubMedSearch : Rial-Crestelo_2017_J.Clin.Lipidol_11_1475 |
| PubMedID: 28942093 |
| Gene_locus related to this paper: human-LCAT |
| Gene_locus related to this paper: human-LCAT |
Rial-Crestelo D, Santos-Recuero I, Julve J, Blanco-Vaca F, Torralba M (2017)
A novel homozygous mutation causing lecithin-cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia
J Clin Lipidol
11 :1475
Rial-Crestelo D, Santos-Recuero I, Julve J, Blanco-Vaca F, Torralba M (2017)
J Clin Lipidol
11 :1475