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The genetic spectrum of familial hypercholesterolemia in Pakistan
BACKGROUND: Familial hypercholesterolemia (FH) is an autosomal dominant disease caused by mutations in the genes coding for the low density lipoprotein receptor (LDLR), proprotein convertase subtilisin/kexin type-9 (PCSK9) or apo-lipoprotein B-100 (APOB). The aim of the present work was to determine...
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| Main Authors: | , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2013
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3701840/ https://ncbi.nlm.nih.gov/pubmed/23535506 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.cca.2013.03.017 |
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