Varaico: Literature-Extracted Genetic Variants

Gene:PCSK9
Variant:p.G227G
Back to variants list

PCSK9

NM_174936.4:p.G227G

Associated Papers

Efficacy, Safety, and Tolerability of Inclisiran in Patients With Homozygous Familial Hypercholesterolemia: Results From the ORION-5 Randomized Clinical Trial.

Raal F et al.

Circulation, 2024

37850379 (PubMed )
Supplement: cir-149-354-s001.pdf

Genetic spectrum of familial hypercholesterolemia and correlations with clinical expression: Implications for diagnosis improvement.

Di Taranto MD et al.

Clinical Genetics, 2021

Population specific genetic heterogeneity of familial hypercholesterolemia in South Africa.

Smyth N et al.

Current Opinion in Lipidology, 2018

Spectrum of mutations in Italian patients with familial hypercholesterolemia: New results from the LIPIGEN study.

Pirillo A et al.

Atherosclerosis. Supplements, 2017

The genetic spectrum of familial hypercholesterolemia in south-eastern Poland.

Sharifi M et al.

Metabolism: Clinical and Experimental, 2016

Inhibition of PCSK9 with evolocumab in homozygous familial hypercholesterolaemia (TESLA Part B): a randomised, double-blind, placebo-controlled trial.

Raal FJ et al.

Lancet (london, England), 2015

Ezetimibe in the management of homozygous familial hypercholesterolaemia.

Mansfield BS et al.

Journal of Clinical Lipidology, 0

Select a paper to view details
UCSC Genome Browser·Imprint·Privacy·Terms·Feedback·Email Updates·

Regarding the variants extracted from papers and shown text snippets from research papers, the following holds: "Some rights reserved. This work permits non-commercial use, distribution and reproduction in any medium, provided the original author and source are credited."