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Article

Molecular description of familial defective APOB-100 in Malaysia.

Biochemical genetics - 1 Oct 2013

Al-Khateeb Alyaa R, Mohd Mohd Sapawi, Yusof Zukarnai, Zilfalil Bin Alwi

Abstract excerpt

Familial ligand-defective apolipoprotein B-100 is characterized by elevated plasma low-density lipoprotein levels and premature heart disease. This study aims to determine apolipoprotein B gene mutations among Malaysians with clinical diagnoses of familial hypercholesterolemia and to compare the phenotype of patients with apolipoprotein B gene mutations to those with a low-density lipoprotein receptor gene...

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Share to Apolipoprotein B-100
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Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Hyperlipoproteinemia Type II

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Share to Mutation, Missense

Share to Receptors, LDL

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Source

Identifiers

PMID: 23775634
DOI: 10.1007/s10528-013-9609-6

Genes

APOB

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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