Pathogenicity assessment of genetic variants identified in patients with severe hypertriglyceridemia: Novel cases of familial chylomicronemia syndrome from the Dyslipidemia Registry of the Spanish Atherosclerosis Society

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Abstract
No abstract available
Funding Information
  • Regional Government of Andalucia Department of Health and Families Progress and Health Foundation (PIN-0180-2018)
  • Government of Andalusia (CTS-159)
  • Swedish Orphan Biovitrum AB publ
  • Suomen Kardiologinen Seura
  • Hospital universitario la paz
  • Fundación General Universidad de La Laguna

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