Varaico: Literature-Extracted Genetic Variants

Gene:PCYT2
Variant:p.K319N
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PCYT2

NM_001184917.3:p.K319N

Associated Papers

ClinPrior: an algorithm for diagnosis and novel gene discovery by network-based prioritization.

Schlüter A et al.

Genome Medicine, 2023

Axonal Polyneuropathy in 2 Brothers With a Homozygous Missense Variant in the First Catalytic Domain of PCYT2.

Leonardis L et al.

Neurology. Genetics, 2022

Defective phosphatidylethanolamine biosynthesis leads to a broad ataxia-spasticity spectrum.

Kaiyrzhanov R et al.

Brain : a Journal of Neurology, 2021

Expanding the clinical and genetic spectrum of PCYT2-related disorders.

Vélez-Santamaría V et al.

Brain : a Journal of Neurology, 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."