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.
Aldizkaria:
BMC Medical Genetics

ISSN: 1471-2350

Argitalpen urtea: 2012

Alea: 13

Mota: Artikulua

DOI: 10.1186/1471-2350-13-106 GOOGLE SCHOLAR lock_openSarbide irekia editor

Garapen Iraunkorreko Helburuak

Datuen iturria: Scopus