Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism (Q35197226)

7 August 2017

Genetic heterogeneity in Leber hereditary optic neuroretinopathy revealed by mitochondrial DNA polymorphism (English)

1 reference

7 August 2017

0 references

1 reference

Vilkki J

1

1 reference

7 August 2017

Savontaus ML

series ordinal

2

1 reference

7 August 2017

Nikoskelainen EK

series ordinal

3

1 reference

7 August 2017

language of work or name

English

0 references

publication date

1 August 1989

1 reference

American Journal of Human Genetics

7 August 2017

1 reference

7 August 2017

45

1 reference

7 August 2017

2

1 reference

7 August 2017

206-211

1 reference

describes a project that uses

7 August 2017

1 reference

LEBER'S DISEASE IN THE NETHERLANDS.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

Sequence and organization of the human mitochondrial genome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

Maternally inherited mitochondrial myopathy and myoclonic epilepsy.

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

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

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

URF6, last unidentified reading frame of human mtDNA, codes for an NADH dehydrogenase subunit

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

Leber's hereditary optic neuropathy: mitochondrial and biochemical studies on muscle biopsies

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

Deletions of mitochondrial DNA in Kearns-Sayre syndrome

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

13 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683352

Mitochondrial inheritance in a mitochondrially mediated disease

13 July 2018

1 reference

12 December 2020

Leber's hereditary optic neuroretinopathy, a mitochondrial disease?

1 reference

12 December 2020

The inheritance of Leber's disease. A genealogical follow-up study

1 reference

12 December 2020

Mitochondrial myopathies

1 reference

12 December 2020

Leber's hereditary optic neuroretinopathy, a maternally inherited disease. A genealogic study in four pedigrees

1 reference

12 December 2020

Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

1 reference

12 December 2020

Human mitochondrial DNA types in Finland

1 reference

12 December 2020

Identifiers

PMCID

1683352

1 reference

7 August 2017

1 reference