Real-time quantitative PCR analysis of mitochondrial DNA content. (Q54392675)

29 May 2018

title

Real-time quantitative PCR analysis of mitochondrial DNA content. (English)

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29 May 2018

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Victor Venegas

1

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29 May 2018

Jing Wang

series ordinal

2

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29 May 2018

David Dimmock

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3

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29 May 2018

Lee-Jun Wong

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4

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publication date

1 January 2011

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Current protocols in human genetics / editorial board, Nicholas C, Dracapoli ... [et al.]

published in

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volume

Chapter 19

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page(s)

Unit 19.7.

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Mutations in COX15 produce a defect in the mitochondrial heme biosynthetic pathway, causing early-onset fatal hypertrophic cardiomyopathy

cites work

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https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Simultaneous detection and quantification of mitochondrial DNA deletion(s), depletion, and over-replication in patients with mitochondrial disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Mutation of RRM2B, encoding p53-controlled ribonucleotide reductase (p53R2), causes severe mitochondrial DNA depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh-like encephalomyopathy, dystonia and deafness.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Clinical and molecular features of mitochondrial DNA depletion due to mutations in deoxyguanosine kinase.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Quantitative evaluation of the mitochondrial DNA depletion syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

New mutations in TK2 gene associated with mitochondrial DNA depletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Recessive Twinkle mutations in early onset encephalopathy with mtDNA depletion.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Simultaneous detection of mitochondrial DNA depletion and single-exon deletion in the deoxyguanosine gene using array-based comparative genomic hybridisation.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Ribonucleotide reduction is a cytosolic process in mammalian cells independently of DNA damage

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Mitochondrial neurogastrointestinal encephalopathy due to mutations in RRM2B.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Molecular analysis for mitochondrial DNA disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Disorders of nuclear-mitochondrial intergenomic communication

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Disorders from perturbations of nuclear-mitochondrial intergenomic cross-talk.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Association of mutations in SCO2, a cytochrome c oxidase assembly gene, with early fetal lethality.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Mutations in the MPV17 gene are responsible for rapidly progressive liver failure in infancy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

Molecular and clinical genetics of mitochondrial diseases due to POLG mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2F0471142905.HG1907S68

10.1002/0471142905.HG1907S68

21 January 2018

Identifiers

DOI

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29 May 2018

PubMed ID

21234878

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29 May 2018