Cita APA

Dussaillant, C. (., Serrano, V. (., Maiz, A. (., Eyheramendy, S. (., Cataldo, L. (. R., Chavez, M. (., . . . Santos, J. (. L. (2012). APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family.

Citación estilo Chicago

Dussaillant, C. (Catalina)|||/items/f10b4c2f-9c37-4a0d-a91b-5c71cf23bb3b, et al. APOA5 Q97X Mutation Identified Through Homozygosity Mapping Causes Severe Hypertriglyceridemia in a Chilean Consanguineous Family. 2012.

Cita MLA

Dussaillant, C. (Catalina)|||/items/f10b4c2f-9c37-4a0d-a91b-5c71cf23bb3b, et al. APOA5 Q97X Mutation Identified Through Homozygosity Mapping Causes Severe Hypertriglyceridemia in a Chilean Consanguineous Family. 2012.