(Q38493565)

3 September 2017

title

Mutations in ND subunits of complex I are an important genetic cause of childhood mitochondrial encephalopathies (English)

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3 September 2017

Byung Chan Lim

1

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3 September 2017

Jun Dong Park

2

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3 September 2017

Hee Hwang

3

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3 September 2017

Ki Joong Kim

4

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3 September 2017

Yong Seung Hwang

5

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3 September 2017

Jong-Hee Chae

6

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3 September 2017

Jung-Eun Cheon

7

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3 September 2017

In One Kim

8

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3 September 2017

Ran Lee

9

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3 September 2017

Han Ku Moon

10

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3 September 2017

publication date

1 July 2009

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Journal of Child Neurology

3 September 2017

published in

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3 September 2017

volume

24

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3 September 2017

issue

7

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3 September 2017

page(s)

828-832

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Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy

3 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

A novel mtDNA mutation in the ND5 subunit of complex I in two MELAS patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Bilateral striatal necrosis associated with a novel mutation in the mitochondrial ND6 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Novel mitochondrial DNA ND5 mutation in a patient with clinical features of MELAS and MERRF.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

A missense mutation in the mitochondrial ND5 gene associated with a Leigh-MELAS overlap syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Recurrent de novo mitochondrial DNA mutations in respiratory chain deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

A novel ND3 mitochondrial DNA mutation in three Korean children with basal ganglia lesions and complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Cytochrome c oxidase deficiency in Leigh syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Maternal inheritance and the evaluation of oxidative phosphorylation diseases

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Molecular diagnostics of mitochondrial disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Novel mutations of ND genes in complex I deficiency associated with mitochondrial encephalopathy

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Progressive mitochondrial disease resulting from a novel missense mutation in the mitochondrial DNA ND3 gene.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

De novo mutations in the mitochondrial ND3 gene as a cause of infantile mitochondrial encephalopathy and complex I deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Fulminant neurological deterioration in a neonate with Leigh syndrome due to a maternally transmitted missense mutation in the mitochondrial ND3 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

An enhanced MITOMAP with a global mtDNA mutational phylogeny

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

The mitochondrial DNA G13513A MELAS mutation in the NADH dehydrogenase 5 gene is a frequent cause of Leigh-like syndrome with isolated complex I deficiency.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

Leigh syndrome caused by mitochondrial DNA G13513A mutation: frequency and clinical features in Japan

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F0883073808331085

21 January 2018

Identifiers

DOI

10.1177/0883073808331085

1 reference

3 September 2017

1 reference