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Molecular Characterization of Iranian Patients with Possible Familial Hypercholesterolemia
Familial hypercholesterolemia (FH) is an autosomal dominant disorder of lipoprotein metabolism caused mainly by mutations in the low-density lipoprotein receptor (LDLR) and apolipoprotein B 100 (APOB) genes. Until now, the molecular basis of FH has been demonstrated in detail in many populations, bu...
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| Main Authors: | , , , , , |
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| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Springer-Verlag
2011
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| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3162949/ https://ncbi.nlm.nih.gov/pubmed/22754187 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s12291-011-0113-7 |
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