APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
Titel:
APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family
Auteur:
Dussaillant, Catalina Serrano, Valentina Maiz, Alberto Eyheramendy, Susana Cataldo, Luis Rodrigo Chavez, Matías Smalley, Susan V Fuentes, Marcela Rigotti, Attilio Rubio, Lorena Lagos, Carlos F Martinez, José Alfredo Santos, José Luis