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Article

A systematic review of LDLR, PCSK9, and APOB variants in Asia.

Atherosclerosis - 1 Jul 2020

Mahdieh Nejat, Heshmatzad Katayoun, Rabbani Bahareh

Abstract excerpt

BACKGROUND AND AIMS: Genetic identification is a public health care concern for management of familial hypercholesterolemia (FH) associated cardiovascular morbidity and mortality. This study presents the spectrum and distribution of LDLR, APOB, PCSK9 gene mutations in Asia. METHODS: Databases were searched for English papers from 1950 to 2019. The spectrum of the variants was investigated in 8994 FH families in...

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PMID: 32629184
DOI: 10.1016/j.atherosclerosis.2020.05.004

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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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