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Complex phenotype of hypercholesterolaemia in a family with both ABCG8 and APOB mutations
Complex phenotype of hypercholesterolaemia in a family with both ABCG8 and APOB mutations
2017
Gonçalo Padeira
Inês Gomes
C Correia
Carla Valongo
Ana Catarina Alves
Ana Margarida Medeiros
Mafalda Bourbon
Ana C. M. Ferreira
Keywords:
Genetics
ABCG8
Familial hypercholesterolemia
Apolipoprotein B
Phenotype
Biology
Correction
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