Varaico: Literature-Extracted Genetic Variants

Gene:RRM2B
Variant:p.M282I
Back to variants list

RRM2B

NM_015713.5:p.M282I

Associated Papers

Investigating the safety and efficacy of deoxycytidine/deoxythymidine in mitochondrial DNA depletion disorders: phase 2 open-label trial.

Berrahmoune S et al.

Journal of Neurology, 2025

Mitochondrial Dysfunction in Sickle Cell Trait Carriers With Exertional Collapse.

Cofer KA et al.

Case Reports in Genetics, 2025

Saccharomyces cerevisiae as a Tool for Studying Mutations in Nuclear Genes Involved in Diseases Caused by Mitochondrial DNA Instability.

Gilea AI et al.

Genes, 2021

Collated mutations in mitochondrial DNA (mtDNA) depletion syndrome (excluding the mitochondrial gamma polymerase, POLG1).

Poulton J et al.

Biochimica Et Biophysica Acta, 2009

Mitochondrial DNA depletion syndrome due to mutations in the RRM2B gene.

Bornstein B et al.

Neuromuscular Disorders : Nmd, 2008

Variability in Cochlear Implantation Outcomes in a Large German Cohort With a Genetic Etiology of Hearing Loss.

Tropitzsch A et al.

Ear and Hearing, 0

37438890 (PubMed )
Supplement: aud-44-1464-s001.pdf
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."