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Article

Complete Apo AI deficiency in an Iraqi Mandaean family: case studies and review of the literature.

Journal of clinical lipidology - 1 Jan 2000

Al-Sarraf Ahmad, Al-Ghofaili Khalid, Sullivan David R, Wasan Kishor M, Hegele Robert, Frohlich Jiri

Abstract excerpt

Complete apo A1 deficiency is a rare genetic disorder that has been associated with premature atherosclerosis. We describe a family of Iraqi Mandaean background with complete apo A1 deficiency caused by a new nonsense mutation in the APOA1 gene. Interestingly, there were marked differences in the clinical presentation of the two homozygotes in this family. A 35-year-old woman presented with xanthelasmas and...

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Share to Apolipoprotein A-I
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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Share to Hydroxymethylglutaryl-CoA Reductase Inhibitors

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Source

Identifiers

PMID: 21122686
DOI: 10.1016/j.jacl.2010.05.001

Genes

APOA1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

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