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Identification and characterization of two novel mutations in the LPL gene causing type I hyperlipoproteinemia.
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- Pingitore, Piero, 1986 (author)
- Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine
- Lepore, Saverio Massimo (author)
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- Pirazzi, Carlo (author)
- Gothenburg University,Göteborgs universitet,Institutionen för medicin, avdelningen för molekylär och klinisk medicin,Institute of Medicine, Department of Molecular and Clinical Medicine
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- Valenti, Luca (author)
- Berge, Knut Erik (author)
- Retterstøl, Kjetil (author)
- Leren, Trond P (author)
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- (creator_code:org_t)
- Elsevier BV, 2016
- 2016
- English.
- In: Journal of clinical lipidology. - : Elsevier BV. - 1933-2874. ; 10:4, s. 816-23
- Journal article (peer-reviewed)
Abstract
Subject headings
Close
- Type 1 hyperlipoproteinemia is a rare autosomal recessive disorder most often caused by mutations in the lipoprotein lipase (LPL) gene resulting in severe hypertriglyceridemia and pancreatitis.
Subject headings
- MEDICIN OCH HÄLSOVETENSKAP -- Klinisk medicin -- Kardiologi (hsv//swe)
- MEDICAL AND HEALTH SCIENCES -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)
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- ref (subject category)
- art (subject category)
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