Complex phenotype of hypercholesterolaemia in a family with both ABCG8 and APOB mutations


Poster presented at


Gonçalo Padeira, Inés Gomes, C. Correia, C. Valongo, A. Alves, A. Medeiros, M. Bourbon, Ana C. M. Ferreira
2017 Mar

Semantic Scholar Repositório INSA
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APA   Click to copy
Padeira, G., Gomes, I., Correia, C., Valongo, C., Alves, A., Medeiros, A., … Ferreira, A. C. M. (2017). Complex phenotype of hypercholesterolaemia in a family with both ABCG8 and APOB mutations.


Chicago/Turabian   Click to copy
Padeira, Gonçalo, Inés Gomes, C. Correia, C. Valongo, A. Alves, A. Medeiros, M. Bourbon, and Ana C. M. Ferreira. “Complex Phenotype of Hypercholesterolaemia in a Family with Both ABCG8 and APOB Mutations,” 2017.


MLA   Click to copy
Padeira, Gonçalo, et al. Complex Phenotype of Hypercholesterolaemia in a Family with Both ABCG8 and APOB Mutations. 2017.


BibTeX   Click to copy

@conference{gon2017a,
  title = {Complex phenotype of hypercholesterolaemia in a family with both ABCG8 and APOB mutations},
  year = {2017},
  month = mar,
  author = {Padeira, Gonçalo and Gomes, Inés and Correia, C. and Valongo, C. and Alves, A. and Medeiros, A. and Bourbon, M. and Ferreira, Ana C. M.},
  month_numeric = {3}
}


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