Exome sequencing reveals novel functional mutations in APOB causing Familial Hypercholesterolaemia


Poster presented at The European Human Genetics Conference 2015. Glasgow, UK on 6-9 June 2015


A. Alves, A. Medeiros, A. Etxebarria, A. Benito-Vicente, César Martín, M. Bourbon
2015 Jun

Semantic Scholar Repositório INSA
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Cite

APA   Click to copy
Alves, A., Medeiros, A., Etxebarria, A., Benito-Vicente, A., Martín, C., & Bourbon, M. (2015). Exome sequencing reveals novel functional mutations in APOB causing Familial Hypercholesterolaemia.


Chicago/Turabian   Click to copy
Alves, A., A. Medeiros, A. Etxebarria, A. Benito-Vicente, César Martín, and M. Bourbon. “Exome Sequencing Reveals Novel Functional Mutations in APOB Causing Familial Hypercholesterolaemia,” 2015.


MLA   Click to copy
Alves, A., et al. Exome Sequencing Reveals Novel Functional Mutations in APOB Causing Familial Hypercholesterolaemia. 2015.


BibTeX   Click to copy

@conference{a2015a,
  title = {Exome sequencing reveals novel functional mutations in APOB causing Familial Hypercholesterolaemia},
  year = {2015},
  month = jun,
  author = {Alves, A. and Medeiros, A. and Etxebarria, A. and Benito-Vicente, A. and Martín, César and Bourbon, M.},
  month_numeric = {6}
}


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