(Q34386660)

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Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations (English)

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

based on heuristic

inferred from title

hereditary optic neuropathy

1 reference

based on heuristic

inferred from title

author name string

Brown MD

1

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Torroni A

2

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Reckord CL

3

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Wallace DC

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

publication date

1 January 1995

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

4

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

311-325

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

Molecular basis of mitochondrial DNA disease

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

21 January 2018

Iatrogenic Creutzfeldt-Jakob disease: an example of the interplay between ancient genes and modern medicine

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

21 January 2018

Sequence and organization of the human mitochondrial genome

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic heterogeneity and mitochondrial DNA heteroplasmy in Leber's hereditary optic neuropathy.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

The spectrum of mitochondrial DNA mutations in families with Leber hereditary optic neuroretinopathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Molecular insight into the asymmetric distribution of pathogenetic human mitochondrial DNA deletions

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytochrome b mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Cytochrome c oxidase mutations in Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's hereditary optic neuropathy. Clinical manifestations of the 3460 mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Leber's hereditary optic neuropathy. Clinical manifestations of the 15257 mutation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

High frequency of mutations at position 11778 in mitochondrial ND4 gene in Japanese families with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Diseases of the mitochondrial DNA.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.1380060405

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1002/HUMU.1380060405

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

1 August 2017

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