Загрузка...
Severe xanthomatosis associated with familial apolipoprotein E deficiency.
AIM: To present the clinical, dermatological, and histological features of a patient with generalised xanthomatosis, familial apolipoprotein (apo) E deficiency, and unusual type III hyperlipoproteinaemia (HLP). METHODS: The underlying molecular defect was disclosed using molecular biological techniq...
Сохранить в:
| Главный автор: | |
|---|---|
| Формат: | Artigo |
| Язык: | Inglês |
| Опубликовано: |
1996
|
| Предметы: | |
| Online-ссылка: | https://ncbi.nlm.nih.gov/pmc/articles/PMC499646/ https://ncbi.nlm.nih.gov/pubmed/9038735 |
| Метки: |
Добавить метку
Нет меток, Требуется 1-ая метка записи!
|