APOA5 Q97x Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family. BMC Med Genet 2012 13, 106.
Authors
Dussaillant C, Serrano V, Eyheramendi S, Smalley SV, Maiz A, Chavez M, Martinez JA, Cataldo LR, Lagos CF, Santos JL.