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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 |