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.
Revue:
BMC Medical Genetics

ISSN: 1471-2350

Année de publication: 2012

Volumen: 13

Type: Article

DOI: 10.1186/1471-2350-13-106 GOOGLE SCHOLAR lock_openAccès ouvert editor
La source de données: Scopus