(Q68799656)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

title

Mitochondria and Leber's hereditary optic neuropathy (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

hereditary optic neuropathy

27 September 2019

main subject

1 reference

N J Newman

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

D C Wallace

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

language of work or name

English

0 references

publication date

1 June 1990

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Ophthalmology

27 September 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

volume

109

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

page(s)

726-730

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

issue

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

Human retinoblastoma susceptibility gene: cloning, identification, and sequence.

27 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Molecular genetics of inherited variation in human color vision

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

A point mutation of the rhodopsin gene in one form of retinitis pigmentosa

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

At least two mutant alleles of ornithine delta-aminotransferase cause gyrate atrophy of the choroid and retina in Finns.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Mitochondrial DNA mutations and neuromuscular disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

The mitochondrial genome--breaking the magic circle

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Maternal inheritance of human mitochondrial DNA

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Maternal inheritance of mitochondrial DNA polymorphisms in cultured human fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Neurological studies in families with Leber's optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Ocular Fundus in Acute Leber Optic Neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

The early phase in Leber hereditary optic atrophy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Leber's optic neuropathy: clinical and visual evoked response studies in asymptomatic and symptomatic members of a 4-generation family

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Bilateral optic neuropathy with remission in young men. Variation on a theme by Leber?

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Leber's disease and dystonia: a mitochondrial disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

A new manifestation of Leber's disease and a new explanation for the agency responsible for its unusual pattern of inheritance

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Mitochondrial DNA mutation in family with Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

Variable genotype of Leber's hereditary optic neuropathy patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0002-9394%2814%2972445-6

10.1016/S0002-9394(14)72445-6

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2346203%20AND%20SRC:MED&resulttype=core&format=json

27 September 2019

1 reference