Disruption of LDL but not VLDL clearance in autosomal recessive hypercholesterolemia

Genetic defects in LDL clearance result in severe hypercholesterolemia and premature atherosclerosis. Mutations in the LDL receptor (LDLR) cause familial hypercholesterolemia (FH), the most severe form of genetic hypercholesterolemia. A phenocopy of FH, autosomal recessive hypercholesterolemia (ARH)...

Полное описание

Сохранить в:
Библиографические подробности
Главные авторы: Jones, Christopher, Garuti, Rita, Michaely, Peter, Li, Wei-Ping, Maeda, Nobuyo, Cohen, Jonathan C., Herz, Joachim, Hobbs, Helen H.
Формат: Artigo
Язык:Inglês
Опубликовано: American Society for Clinical Investigation 2007
Предметы:
Research Article
Online-ссылка:https://ncbi.nlm.nih.gov/pmc/articles/PMC1716209/
https://ncbi.nlm.nih.gov/pubmed/17200716
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI29415
Метки: Добавить метку
Нет меток, Требуется 1-ая метка записи!

Схожие документы