Genetics in familial hypercholesterolaemia – from genetic research to new guidelines
Familial Hypercholesterolaemia (FH) is genetic disorder touching up to 1 to 250 people, increasing the risk of atherosclerotic cardiovascular disease risk and early death by 3–13 times. The majority of mutations are autosomal dominant among 3 genes related to cholesterole metabolism: LDL‑receptor (L...
में बचाया:
| मुख्य लेखकों: | , , |
|---|---|
| स्वरूप: | Artigo |
| भाषा: | Inglês |
| प्रकाशित: |
Poznan University of Medical Sciences
2019-04-01
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| श्रृंखला: | Journal of Medical Science |
| विषय: | |
| ऑनलाइन पहुंच: | https://jms.ump.edu.pl/index.php/JMS/article/view/245 |
| टैग: |
कोई टैग नहीं, इस रिकॉर्ड को टैग करने वाले पहले व्यक्ति बनें!
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