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Dive into the research topics of 'APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family'. Together they form a unique fingerprint.- Sort by
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Catalina Dussaillant, Valentina Serrano, Alberto Maiz, Susana Eyheramendy, Luis R. Cataldo, Matías Chavez, Susan V. Smalley, Marcela Fuentes, Attilio Rigotti, Lorena Rubio, Carlos F. Lagos, José A. Martinez, José L. Santos
Research output: Contribution to journal › Article › peer-review