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Rare LPL gene missense mutation in an infant with hypertriglyceridemia
BACKGROUND: Severe hypertriglyceridemia usually results from a combination of genetic and environmental factors and is most often attributable to mutations in the lipoprotein lipase (LPL) gene. OBJECTIVES: The aim of this study was to identify rare mutations in the LPL gene causing severe hypertrigl...
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| Publicado no: | J Clin Lab Anal |
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| Main Authors: | , , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
John Wiley and Sons Inc.
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6817128/ https://ncbi.nlm.nih.gov/pubmed/29479812 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jcla.22414 |
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