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Current Treatment of Familial Hypercholesterolaemia
Familial hypercholesterolaemia is an autosomal-dominant disorder associated with mutations in the LDL receptor gene resulting in markedly elevated plasma low-density lipoprotein cholesterol levels. FH is significantly underrecognised with as many as 1 in 300 having the heterozygous form and 1 in 1 m...
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| Publicado no: | Eur Cardiol |
|---|---|
| Main Authors: | , , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Radcliffe Cardiology
2014
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6159444/ https://ncbi.nlm.nih.gov/pubmed/30310490 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.15420/ecr.2014.9.2.76 |
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