The clinical spectrum and natural history of early-onset diseases due to DNA polymerase gamma mutations | Genetics in Medicine
POLG - Wikipedia
POLG-dependent changes in mitochondrial gene expression are not... | Download Scientific Diagram
POLG - Wikipedia
Nucleotide substitutions in POLG . ( A ) Human POLG gene on chromosome... | Download Scientific Diagram
i>POLG </i>Mutations Are Probably Rare in the Han Chinese Population
DNA Polymerase Gamma Recovers Mitochondrial Function and Inhibits Vascular Calcification by Interacted with p53
POLG mutation sites were conserved. (a) Domains and mutation sites in... | Download Scientific Diagram
Nucleotide substitutions in POLG . ( A ) Human POLG gene on chromosome... | Download Scientific Diagram
Figure 3 from Molecular diagnosis of Alpers syndrome. | Semantic Scholar
POLG-related disorders and their neurological manifestations | Nature Reviews Neurology
POLG Gene - GeneCards | DPOG1 Protein | DPOG1 Antibody
Pathogenicity in POLG syndromes: DNA polymerase gamma pathogenicity prediction server and database - ScienceDirect
Epilepsy due to mutations in the mitochondrial polymerase gamma (POLG) gene: A clinical and molecular genetic review - Anagnostou - 2016 - Epilepsia - Wiley Online Library
i>POLG </i>Mutations Are Probably Rare in the Han Chinese Population
Home - The POLG Foundation
PPFIA4 mutation: A second hit in POLG related disease? - ScienceDirect
Genes | Free Full-Text | De Novo Development of mtDNA Deletion Due to Decreased POLG and SSBP1 Expression in Humans
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
POLG mutations characterized in this study. A, the location of the six... | Download Scientific Diagram
Schematic representation of chromosome 15 showing the position of POLG... | Download Scientific Diagram
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
Stem cell derived astrocytes with POLG mutations and mitochondrial dysfunction including abnormal NAD+ metabolism is toxic for neurons | bioRxiv
