APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
Keywords:
Hypertriglyceridemia
Genetic
Chylomicronemia
Mutation
Homozygosity mapping
APOA5
Publisher:
BioMed Central
Citation:
Dussaillant C, Serrano V, Maiz A, Eyheramendy S, Cataldo LR, Chavez M, et al. APOA5 Q97X mutation identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family. BMC Med Genet 2012 Nov 15;13:106
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