APOA5 Q97X Mutation Identified through homozygosity mapping causes severe hypertriglyceridemia in a Chilean consanguineous family

  1. Dussaillant, C.
  2. Serrano, V.
  3. Maiz, A.
  4. Eyheramendy, S.
  5. Cataldo, L.R.
  6. Chavez, M.
  7. Smalley, S.V.
  8. Fuentes, M.
  9. Rigotti, A.
  10. Rubio, L.
  11. Lagos, C.F.
  12. Martinez, J.A.
  13. Santos, J.L.
Revista:
BMC Medical Genetics

ISSN: 1471-2350

Ano de publicación: 2012

Volume: 13

Tipo: Artigo

DOI: 10.1186/1471-2350-13-106 GOOGLE SCHOLAR lock_openAcceso aberto editor