(Q49021635)

17 February 2018

title

Leigh syndrome in an infant resulting from mitochondrial DNA depletion. (English)

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17 February 2018

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Absalon MJ

1

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17 February 2018

Harding CO

2

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17 February 2018

Fain DR

3

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17 February 2018

Li L

4

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17 February 2018

Mack KJ

5

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17 February 2018

publication date

1 January 2001

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17 February 2018

published in

Pediatric Neurology

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17 February 2018

volume

24

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17 February 2018

issue

1

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17 February 2018

page(s)

60-63

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17 February 2018

Getting to the nucleus of mitochondrial disorders: identification of respiratory chain-enzyme genes causing Leigh syndrome

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Leigh syndrome: clinical features and biochemical and DNA abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Clinical heterogeneity associated with mitochondrial DNA depletion in muscle

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Clinical manifestations of mitochondrial DNA depletion

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Subacute necrotizing encephalomyelopathy in an infant

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Biochemical study in 28 children with lactic acidosis, in relation to Leigh's encephalomyelopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Magnetic resonance imaging in subacute necrotizing encephalomyelopathy (Leigh's disease).

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Deficiency of respiratory chain complex I is a common cause of Leigh disease.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

The first nuclear-encoded complex I mutation in a patient with Leigh syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Mutations of SURF-1 in Leigh disease associated with cytochrome c oxidase deficiency

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Liver failure associated with mitochondrial DNA depletion

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Mitochondrial myopathy of childhood associated with depletion of mitochondrial DNA

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Mitochondrial DNA depletion: prevalence in a pediatric population referred for neurologic evaluation.

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Low levels of mitochondrial transcription factor A in mitochondrial DNA depletion

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

Mitochondrial transcription factor A is necessary for mtDNA maintenance and embryogenesis in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0887-8994%2800%2900226-5

7 January 2021

10.1016/S0887-8994(00)00226-5

Identifiers

DOI

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17 February 2018

1 reference

17 February 2018