A novel homozygous mutation causing lecithin–cholesterol acyltransferase deficiency in a proband of Romanian origin with a record of extreme gestational hyperlipidemia
- Rial-Crestelo, D.
- Santos-Recuero, I.
- Julve, J.
- Blanco-Vaca, F.
- Torralba, M.
ISSN: 1876-4789, 1933-2874
Année de publication: 2017
Volumen: 11
Número: 6
Pages: 1475-1479.e3
Type: Article