Varaico: Literature-Extracted Genetic Variants

Gene:NEFL
Variant:p.A149V
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NEFL

NM_006158.5:p.A149V

Associated Papers

O-GlcNAcylation regulates neurofilament-light assembly and function and is perturbed by Charcot-Marie-Tooth disease mutations.

Huynh DT et al.

Nature Communications, 2023

Effect of Neurodegenerative Mutations in the NEFL Gene on Thermal Denaturation of the Neurofilament Light Chain Protein.

Nefedova VV et al.

Biochemistry. Biokhimiia, 2023

O-GlcNAcylation regulates neurofilament-light assembly and function and is perturbed by Charcot-Marie-Tooth disease mutations.

Huynh DT et al.

Biorxiv : the Preprint Server for Biology, 2023

The 2022 Lady Estelle Wolfson lectureship on neurofilaments.

Petzold A

Journal of Neurochemistry, 2022

A review and analysis of the clinical literature on Charcot-Marie-Tooth disease caused by mutations in neurofilament protein L.

Stone EJ et al.

Cytoskeleton (hoboken, N.j.), 2021

A novel pathogenic variant of NEFL responsible for deafness associated with peripheral neuropathy discovered through next-generation sequencing and review of the literature.

Lerat J et al.

Journal of the Peripheral Nervous System : Jpns, 2019

Absence of NEFL in patient-specific neurons in early-onset Charcot-Marie-Tooth neuropathy.

Sainio MT et al.

Neurology. Genetics, 2018

Genetic and clinical characteristics of NEFL-related Charcot-Marie-Tooth disease.

Horga A et al.

Journal of Neurology, Neurosurgery, and Psychiatry, 2017

Muscle pathology without severe nerve pathology in a new mouse model of Charcot-Marie-Tooth disease type 2E.

Shen H et al.

Human Molecular Genetics, 2011

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