(Q41136397)

27 September 2017

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title

The other human genome: mitochondrial DNA and disease (English)

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27 September 2017

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Johns DR

1

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27 September 2017

language of work or name

English

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publication date

1 October 1996

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27 September 2017

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27 September 2017

volume

2

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27 September 2017

issue

10

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27 September 2017

page(s)

1065-1068

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Mitochondrial DNA and human evolution

27 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Seminars in medicine of the Beth Israel Hospital, Boston. Mitochondrial DNA and disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Identical twins who are discordant for Leber's hereditary optic neuropathy.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Leber's hereditary optic neuropathy masquerading as tobacco-alcohol amblyopia

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Respiration and growth defects in transmitochondrial cell lines carrying the 11778 mutation associated with Leber's hereditary optic neuropathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Mitochondrial diabetes mellitus: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Do defects in mitochondrial energy metabolism underlie the pathology of neurodegenerative diseases?

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

Sequence and organization of the human mitochondrial genome

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Mitochondrial DNA sequence heteroplasmy in the Grand Duke of Russia Georgij Romanov establishes the authenticity of the remains of Tsar Nicholas II

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Molecular basis of mitochondrial DNA disease

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Mitochondrial encephalomyopathies: clinical and molecular analysis

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Atypical clinical presentations associated with the MELAS mutation at position 3243 of human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcripts

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Oxidative damage and mitochondrial decay in aging

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Mutation of a nuclear succinate dehydrogenase gene results in mitochondrial respiratory chain deficiency

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

An autosomal locus predisposing to deletions of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1038%2FNM1096-1065

7 January 2021

Identifiers

DOI

10.1038/NM1096-1065

1 reference

27 September 2017

1 reference