(Q57252080)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20639910%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

title

Genetics: Optic nerve genetics--more than meets the eye (English)

1 reference

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8 February 2020

1

1 reference

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8 February 2020

Ian A. Trounce

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20639910%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

author name string

David A. Mackey

series ordinal

1

0 references

language of work or name

English

0 references

publication date

1 July 2010

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20639910%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

published in

Nature Reviews Neurology

1 reference

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8 February 2020

volume

6

1 reference

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8 February 2020

issue

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20639910%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

page(s)

357-358

1 reference

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https://scigraph.springernature.com/pub.10.1038/nrneurol.2010.77

8 February 2020

exact match

0 references

cites work

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Multi-system neurological disease is common in patients with OPA1 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Critical dependence of neurons on mitochondrial dynamics

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Occurrence of a multiple sclerosis-like illness in women who have a Leber's hereditary optic neuropathy mitochondrial DNA mutation

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Leber's "plus": neurological abnormalities in patients with Leber's hereditary optic neuropathy

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Molecular screening of 980 cases of suspected hereditary optic neuropathy with a report on 77 novel OPA1 mutations.

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Autosomal Dominant Optic Atrophy: Penetrance and Expressivity in Patients With OPA1 Mutations

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Mutations of optineurin in amyotrophic lateral sclerosis

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance

31 March 2020

1 reference

https://api.crossref.org/works/10.1038%2FNRNEUROL.2010.77

Infantile optic atrophy with dominant mode of inheritance: a clinical and genetic study of 19 Danish families

31 March 2020

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/20639910

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NRNEUROL.2010.77

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:20639910%20AND%20SRC:MED&resulttype=core&format=json

8 February 2020

1 reference