Загрузка...
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...
Сохранить в:
| Опубликовано в: : | JIMD Rep |
|---|---|
| Главные авторы: | , , , , |
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
John Wiley & Sons, Inc.
2019
|
| Предметы: | |
| Online-ссылка: | 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 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|