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

Any de publicació: 2012

Volum: 13

Tipus: Article

DOI: 10.1186/1471-2350-13-106 GOOGLE SCHOLAR lock_openAccés obert editor