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Sitosterolemia—10 years observation in two sisters
Familial hypercholesterolemia due to heterozygous low‐density lipoprotein‐receptor mutations is a common inborn errors of metabolism. Secondary hypercholesterolemia due to a defect in phytosterol metabolism is far less common and may escape diagnosis during the work‐up of patients with dyslipidemias...
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| Pubblicato in: | JIMD Rep |
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| Autori principali: | , , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
John Wiley & Sons, Inc.
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6607017/ https://ncbi.nlm.nih.gov/pubmed/31392106 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/jmd2.12038 |
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