Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia
- PMID: 19007591
- PMCID: PMC3423908
- DOI: 10.1016/j.jacc.2008.08.012
Frequent detection of familial hypercholesterolemia mutations in familial combined hyperlipidemia
Conflict of interest statement
All three authors have no conflict of interest.
Comment on
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Frequency of low-density lipoprotein receptor gene mutations in patients with a clinical diagnosis of familial combined hyperlipidemia in a clinical setting.J Am Coll Cardiol. 2008 Nov 4;52(19):1546-53. doi: 10.1016/j.jacc.2008.06.050. J Am Coll Cardiol. 2008. PMID: 19007590
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