POLG - Wikipedia
Stem cell derived astrocytes with POLG mutations and mitochondrial dysfunction including abnormal NAD+ metabolism is toxic for neurons | bioRxiv
Human DNA Polymerase Gamma Mutation Database
Evidence for a novel overlapping coding sequence in POLG initiated at a CUG start codon | BMC Genomic Data | Full Text
Simplifying the clinical classification of polymerase gamma (POLG) disease based on age of onset; studies using a cohort of 155 cases - Hikmat - 2020 - Journal of Inherited Metabolic Disease - Wiley Online Library
Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review - Anagnostou - 2016 - Epilepsia - Wiley Online Library
Inflammation-induced DNA methylation of DNA polymerase gamma alters the metabolic profile of colon tumors | Cancer & Metabolism | Full Text
DNA polymerase gamma and mitochondrial disease: Understanding the consequence of POLG mutations - ScienceDirect
i>POLG </i>Mutations Are Probably Rare in the Han Chinese Population
POLG - Wikipedia
Genes | Free Full-Text | De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans
Schematic representation of chromosome 15 showing the position of POLG... | Download Scientific Diagram
DNA polymerase gamma and mitochondrial disease: Understanding the consequence of POLG mutations - ScienceDirect
Nucleotide substitutions in POLG . ( A ) Human POLG gene on chromosome... | Download Scientific Diagram
Pathogenicity in POLG syndromes: DNA polymerase gamma pathogenicity prediction server and database - ScienceDirect
The Role of Mitochondrial DNA Mutations in Mammalian Aging | PLOS Genetics
POLG Gene - GeneCards | DPOG1 Protein | DPOG1 Antibody
Novel POLG mutations in progressive external ophthalmoplegia mimicking mitochondrial neurogastrointestinal encephalomyopathy | European Journal of Human Genetics
Figure 3 from Molecular diagnosis of Alpers syndrome. | Semantic Scholar
Genes | Free Full-Text | De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans
The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations | Genetics in Medicine
Genetic analysis of the patient. (A) Sanger sequencing validation of... | Download Scientific Diagram
A perspective on human cell models for POLG-spectrum disorders: advantages and disadvantages of CRISPR-Cas-based vs. patient-der
DNA Polymerase Gamma Recovers Mitochondrial Function and Inhibits Vascular Calcification by Interacted with p53
POLG-dependent changes in mitochondrial gene expression are not... | Download Scientific Diagram
In Vivo Functional Analysis of the Human Mitochondrial DNA Polymerase POLG Expressed in Cultured Human Cells*
IJNS | Free Full-Text | Compound Heterozygosity for a Novel Frameshift Variant Causing Fatal Infantile Liver Failure and Genotype–Phenotype Correlation of POLG c.3286C>T Variant
POLG mutations characterized in this study. A, the location of the six... | Download Scientific Diagram
Home - The POLG Foundation
POLG-related disorders and their neurological manifestations | Nature Reviews Neurology
