|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Advantages and pitfalls of an extended gene panel for investigating complex neurometabolic phenotypes.
|
27604308 |
2016 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population.
|
16401742 |
2006 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
Autosomal recessive mitochondrial ataxic syndrome due to mitochondrial polymerase gamma mutations.
|
15824347 |
2005 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
Bowel obstruction in patients with Alpers-Huttenlocher syndrome.
|
22006280 |
2011 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Clinical and genetic heterogeneity in progressive external ophthalmoplegia due to mutations in polymerase gamma.
|
12975295 |
2003 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Digenic progressive external ophthalmoplegia in a sporadic patient: recessive mutations in POLG and C10orf2/Twinkle.
|
12872260 |
2003 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Early-onset familial parkinsonism due to POLG mutations.
|
16634032 |
2006 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome.
|
15917273 |
2005 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
Functional defects due to spacer-region mutations of human mitochondrial DNA polymerase in a family with an ataxia-myopathy syndrome.
|
15917273 |
2005 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
High-throughput, pooled sequencing identifies mutations in NUBPL and FOXRED1 in human complex I deficiency.
|
20818383 |
2010 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
Infantile hepatocerebral syndromes associated with mutations in the mitochondrial DNA polymerase-gammaA.
|
15689359 |
2005 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
MELAS/SANDO overlap syndrome associated with POLG1 mutations.
|
21647632 |
2012 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE)-like phenotype: an expanded clinical spectrum of POLG1 mutations.
|
21993618 |
2012 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Molecular analysis of ANT1, TWINKLE and POLG in patients with multiple deletions or depletion of mitochondrial DNA by a dHPLC-based assay.
|
16639411 |
2006 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.
|
11431686 |
2001 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Mutation of POLG is associated with progressive external ophthalmoplegia characterized by mtDNA deletions.
|
11431686 |
2001 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO).
|
12707443 |
2003 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
Parieto-occipital lobe epilepsy caused by a POLG1 compound heterozygous A467T/W748S genotype.
|
21515089 |
2011 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Parkinsonism, premature menopause, and mitochondrial DNA polymerase gamma mutations: clinical and molecular genetic study.
|
15351195 |
2004 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Phenotypic spectrum associated with mutations of the mitochondrial polymerase gamma gene.
|
16621917 |
2006 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
POLG mutation presenting with late-onset jerky torticollis.
|
23212759 |
2013 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.
|
15477547 |
2004 |
|
| Entrez Id: |
5428 |
| Gene Symbol: |
POLG |
POLG
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
POLG mutations in neurodegenerative disorders with ataxia but no muscle involvement.
|
15477547 |
2004 |