Common Mutations in LDLR Gene in Familial Hypercholesterolemia
Background and Objective: Familial hypercholesterolemia (FH) is one of the most common inherited familial diseases that cause lipid accumulation in tendons and arteries by increasing the level of low density plasma lipoprotein (LDL). The main cause of FH is a mutation in the low-density lipoprotein...
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| Auteurs principaux: | , , |
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| Format: | Artigo |
| Langue: | Persa |
| Publié: |
Golestan University of Medical Sciences
2022-01-01
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| Collection: | مجله دانشگاه علوم پزشکی گرگان |
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| Accès en ligne: | http://goums.ac.ir/journal/article-1-3977-en.html |
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