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A novel homozygous mutation causing lecithin–cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia
Rial-Crestelo, David, Santos-Recuero, Ildefonso, Julve, Josep, Blanco-Vaca, Francisco, Torralba, MiguelLanguage:
english
Journal:
Journal of Clinical Lipidology
DOI:
10.1016/j.jacl.2017.08.008
Date:
August, 2017
File:
PDF, 1.13 MB
english, 2017