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The common biological basis for common complex diseases: evidence from lipoprotein lipase gene
The lipoprotein lipase (LPL) gene encodes a rate-limiting enzyme protein that has a key role in the hydrolysis of triglycerides. Hypertriglyceridemia, one widely prevalent syndrome of LPL deficiency and dysfunction, may be a risk factor in the development of dyslipidemia, type II diabetes (T2D), ess...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Nature Publishing Group
2010
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2987160/ https://ncbi.nlm.nih.gov/pubmed/19639021 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1038/ejhg.2009.134 |
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