(Q42441777)

31 October 2017

mtDNA depletion myopathy: elucidation of the tissue specificity in the mitochondrial thymidine kinase (TK2) deficiency (English)

1 reference

31 October 2017

1

1 reference

31 October 2017

Avraham Shaag

2

1 reference

PubMed ID

12765840

31 October 2017

Orly Elpeleg

series ordinal

3

1 reference

31 October 2017

1 May 2003

1 reference

Molecular Genetics and Metabolism

31 October 2017

1 reference

31 October 2017

79

1 reference

31 October 2017

1

1 reference

31 October 2017

1-5

1 reference

Mammalian deoxyribonucleoside kinases

31 October 2017

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

The human mitochondrial deoxynucleotide carrier and its role in the toxicity of nucleoside antivirals

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Mitochondrial DNA depletion: mutations in thymidine kinase gene with myopathy and SMA.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Depletion of the other genome-mitochondrial DNA depletion syndromes in humans

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

An X-linked mitochondrial disease affecting cardiac muscle, skeletal muscle and neutrophil leucocytes

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Human thymidine kinase 2: molecular cloning and characterisation of the enzyme activity with antiviral and cytostatic nucleoside substrates

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Rearrangements of human mitochondrial DNA (mtDNA): new insights into the regulation of mtDNA copy number and gene expression

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Mitochondrial DNA maintenance in vertebrates

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Depletion of mitochondrial DNA associated with infantile cholestasis and progressive liver fibrosis.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Molecular mechanisms in mitochondrial DNA depletion syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Clinical manifestations of mitochondrial DNA depletion.

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Navajo neurohepatopathy: a mitochondrial DNA depletion syndrome?

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

Mitochondrial DNA depletion and dGK gene mutations

1 reference

https://api.crossref.org/works/10.1016%2FS1096-7192%2803%2900063-5

7 January 2021

10.1016/S1096-7192(03)00063-5

Identifiers

DOI

1 reference

31 October 2017

1 reference

PubMed ID

12765840