(Q33735635)

29 July 2017

title

Brainstem involvement in Leber's hereditary optic neuropathy: association with the 14,484 mitochondrial DNA mutation (English)

1 reference

hereditary optic neuropathy

29 July 2017

0 references

1 reference

Funalot B

1

1 reference

29 July 2017

Ranoux D

2

1 reference

29 July 2017

Mas JL

3

1 reference

29 July 2017

Garcia C

4

1 reference

29 July 2017

Bonnefont JP

5

1 reference

29 July 2017

language of work or name

English

0 references

publication date

1 November 1996

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

29 July 2017

published in

1 reference

29 July 2017

volume

61

1 reference

29 July 2017

issue

5

1 reference

29 July 2017

page(s)

533-534

1 reference

Pitfalls in the molecular genetic diagnosis of Leber hereditary optic neuropathy (LHON).

29 July 2017

cites work

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074061

Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074061

Central nervous system involvement in Leber's optic neuropathy.

21 June 2018

1 reference

PubMed Central

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1074061

The clinical features of Leber's hereditary optic neuropathy defined by the presence of a pathogenic mitochondrial DNA mutation

30 October 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/8937358

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.61.5.533

1 reference

29 July 2017

1 reference

29 July 2017

1 reference