A novel homozygous mutation causing lecithin–cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia

1. Rial-Crestelo, D.
2. Santos-Recuero, I.
3. Julve, J.
4. Blanco-Vaca, F.
5. Torralba, M.