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    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 by Dussaillant Catalina, Serrano Valentina, Maiz Alberto, Eyheramendy Susana, Cataldo Luis, Chavez Matías, Smalley Susan V, Fuentes Marcela, Rigotti Attilio, Rubio Lorena, Lagos Carlos F, Martinez José, Santos José

    Published 2012
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