Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy (Q33631235)

28 July 2017

Restriction endonuclease analysis of leukocyte mitochondrial DNA in Leber's optic atrophy (English)

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28 July 2017

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Holt IJ

1

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28 July 2017

Miller DH

series ordinal

2

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28 July 2017

Harding AE

series ordinal

3

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28 July 2017

language of work or name

English

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publication date

1 August 1988

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Journal of Neurology, Neurosurgery and Psychiatry

28 July 2017

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28 July 2017

51

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28 July 2017

8

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28 July 2017

1075-1077

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New aspects of the genetic, etiologic, and clinical puzzle of Leber's disease

28 July 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Radiation of human mitochondria DNA types analyzed by restriction endonuclease cleavage patterns

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Maternal inheritance of human mitochondrial DNA

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Polymorphism in mitochondrial DNA of humans as revealed by restriction endonuclease analysis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Leber's Optic Atrophy: A Possible Example of Vertical Transmission of a Slow Virus in Man

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Leber's optic atrophy, a possible example of maternal inheritance.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Six unidentified reading frames of human mitochondrial DNA encode components of the respiratory-chain NADH dehydrogenase

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

The clinical features of mitochondrial myopathy.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Deficiency of thiosulphate sulphurtransferase (rhodanese) in Leber's hereditary optic neuropathy

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Mitochondrial DNA and human evolution

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Human mitochondrial DNA types in two Israeli populations--a comparative study at the DNA level

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Mitochondrial myopathies: deficiencies localized to complex I and complex III of the mitochondrial respiratory chain.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

The mitochondrial electron transport and oxidative phosphorylation system

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Detection of specific sequences among DNA fragments separated by gel electrophoresis

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Labeling deoxyribonucleic acid to high specific activity in vitro by nick translation with DNA polymerase I

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Conservation of genes coding for proteins synthesized in human mitochondria

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Leber's hereditary optic atrophy: a possible defect of cyanide metabolism.

21 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1033117

Leber's optic neuropathy: a clinical and visual evoked potential study of affected and asymptomatic members of a six generation family

30 October 2018

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

12 December 2020

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. I. Fundus findings in asymptomatic family members

1 reference

12 December 2020

Mitochondrial inheritance in a mitochondrially mediated disease

1 reference

12 December 2020

Ophthalmoscopic findings in Leber's hereditary optic neuropathy. II. The fundus findings in the affected family members

1 reference

12 December 2020

Mitochondrial DNA polymorphism in Japanese. I. Analysis with restriction enzymes of six base pair recognition

1 reference

12 December 2020

Mitochondrial myopathies

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12 December 2020

Mitochondrial DNA polymorphism in Japanese. II. Analysis with restriction enzymes of four or five base pair recognition

1 reference

12 December 2020

Leber's disease and dystonia: a mitochondrial disease

1 reference

12 December 2020

Genetic transmission of myoclonus epilepsy with ragged red fibers

1 reference

12 December 2020

Identifiers

DOI

10.1136/JNNP.51.8.1075

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28 July 2017

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28 July 2017

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