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Article

Frequency of low-density lipoprotein receptor gene mutations in patients with a clinical diagnosis of familial combined hyperlipidemia in a clinical setting.

Journal of the American College of Cardiology - 4 Nov 2008

Civeira Fernando, Jarauta Estibaliz, Cenarro Ana, García-Otín Angel L, Tejedor Diego, Zambón Daniel, Mallen Miguel, Ros Emilio, Pocoví Miguel

Abstract excerpt

OBJECTIVES: The purpose of this study was to determine the frequency of mutations in the low-density lipoprotein receptor (LDLR) and apolipoprotein B (APOB) genes in consecutive patients with a clinical diagnosis of familial combined hyperlipidemia (FCH) in a nonresearch setting. BACKGROUND: The...

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Share to Analysis of Variance
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Hyperlipidemia, Familial Combined

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Share to Receptors, LDL

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Source

Identifiers

PMID: 19007590
DOI: 10.1016/j.jacc.2008.06.050

Genes

LDLR
APOB

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19007590-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

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