Varaico: Literature-Extracted Genetic Variants

Gene:MYORG
Variant:p.T265M
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MYORG

NM_020702.5:p.T265M

Associated Papers

A patient with a MYORG variant in primary brain calcification has rapid clinical course and increased calcification volume on an image analyzer.

Hozumi I et al.

Clinical Neurology and Neurosurgery, 2025

Fahr's disease linked to a novel mutation in MYORG variants manifesting as paroxysmal limb stiffness and dysarthria: Case report and literature review.

Zhao T et al.

Molecular Genetics & Genomic Medicine, 2023

A novel MYORG mutation causes primary familial brain calcification with migraine: Case report and literature review.

Song T et al.

Frontiers in Neurology, 2023

The primary familial brain calcification-associated protein MYORG is an α-galactosidase with restricted substrate specificity.

Meek RW et al.

Plos Biology, 2022

36129849 (PubMed )
Supplement: pbio.3001764.s007.pdf

Paroxysmal Kinesigenic Dyskinesia Secondary to Brain Calcification with a Homozygous MYORG Mutation.

Du J et al.

Movement Disorders : Official Journal of the Movement Disorder Society, 2021

The first Japanese case of primary familial brain calcification caused by an MYORG variant.

Kume K et al.

Journal of Human Genetics, 2020

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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."