Varaico: Literature-Extracted Genetic Variants

Gene:OCLN
Variant:p.G406G
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OCLN

NM_001205254.2:p.G406G

Associated Papers

Genetic Mutations in Cell Junction Proteins Associated with Brain Calcification.

Yang D et al.

Movement Disorders : Official Journal of the Movement Disorder Society, 2025

Genetic Testing for Malformations of Cortical Development: A Clinical Diagnostic Study.

Straka B et al.

Neurology. Genetics, 2022

OCLN gene variants identified in three patients with severe neurodevelopmental disorder associated with epilepsy, intellectual disability and malformation of cortical development.

Oner TO et al.

Epileptic Disorders : International Epilepsy Journal With Videotape, 2021

Comprehensive molecular screening strategy of OCLN in band-like calcification with simplified gyration and polymicrogyria.

Jenkinson EM et al.

Clinical Genetics, 2018

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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."