טוען...
Heterozygous familial hypercholesterolaemia in a pair of identical twins: a case report and updated review
BACKGROUND: Familial hypercholesterolaemia (FH) is the most common inherited metabolic disease with an autosomal dominant mode of inheritance. It is characterised by raised serum levels of total cholesterol (TC) and low-density lipoprotein cholesterol (LDL-c), leading to premature coronary artery di...
שמור ב:
| הוצא לאור ב: | BMC Pediatr |
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| Main Authors: | , , , , |
| פורמט: | Artigo |
| שפה: | Inglês |
| יצא לאור: |
BioMed Central
2019
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| נושאים: | |
| גישה מקוונת: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6458607/ https://ncbi.nlm.nih.gov/pubmed/30975109 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s12887-019-1474-y |
| תגים: |
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