Autor:
Dussaillant, Catalina
Serrano Larrea, Valentina.
Maiz Gurruchaga, Manuel Alberto.
Eyheramendy Duerr, Susana.
Cataldo, Luis R.
Smalley, Susan V.
Rigotti Rivera, Attilio.
Rubio, Lorena.
Lagos Arévalo, Carlos Fernando.
Santos Martín, José Luis.
Abstract Background Severe hypertriglyceridemia (HTG) has been linked to defects in LPL, APOC2, APOA5, LMF1 and GBIHBP1 genes. However, a number of severe HTG cases are probably caused by as yet unidentified mutations. Very high triglyceride plasma l...
Enlace original:
https://repositorio.uc.cl/handle/11534/26724
Dussaillant, Catalina
,
Serrano Larrea, Valentina.
,
Maiz Gurruchaga, Manuel Alberto.
,
Eyheramendy Duerr, Susana.
,
Cataldo, Luis R.
,
Smalley, Susan V.
,
Rigotti Rivera, Attilio.
,
Rubio, Lorena.
,
Lagos Arévalo, Carlos Fernando.
,
Santos Martín, José Luis.
,
[APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family]
,
APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family