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Partial LPL deletions: rare copy-number variants contributing towards severe hypertriglyceridemia
Severe hypertriglyceridemia (HTG) is a relatively common form of dyslipidemia with a complex pathophysiology and serious health complications. HTG can develop in the presence of rare genetic factors disrupting genes involved in the triglyceride (TG) metabolic pathway, including large-scale copy-numb...
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| Yayımlandı: | J Lipid Res |
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| Asıl Yazarlar: | , , , , , , , , , , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
The American Society for Biochemistry and Molecular Biology
2019
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| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6824486/ https://ncbi.nlm.nih.gov/pubmed/31519763 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1194/jlr.P119000335 |
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