Progressive reversion of clinical and molecular phenotype in a child with liver mitochondrial DNA depletion. (Q51718920)

10 April 2018

title

Progressive reversion of clinical and molecular phenotype in a child with liver mitochondrial DNA depletion. (English)

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10 April 2018

main subject

mitochondrial DNA

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author name string

Pierre-Henri Ducluzeau

1

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10 April 2018

Alain Lachaux

2

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10 April 2018

Raymonde Bouvier

3

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10 April 2018

Hervé Duborjal

4

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10 April 2018

Georges Stepien

5

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10 April 2018

Dominique Bozon

6

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10 April 2018

Bénédicte Mousson de Camaret

7

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10 April 2018

publication date

1 May 2002

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10 April 2018

published in

Journal of Hepatology

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10 April 2018

volume

36

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10 April 2018

issue

5

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10 April 2018

page(s)

698-703

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10 April 2018

Late-onset mitochondrial DNA depletion: DNA copy number, multiple deletions, and compensation

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Clinical heterogeneity associated with mitochondrial DNA depletion in muscle.

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Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease

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Liver failure associated with mitochondrial DNA depletion

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Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

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Neonatal and delayed-onset liver involvement in disorders of oxidative phosphorylation

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Mitochondrial disorders

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The augmenter of liver regeneration induces mitochondrial gene expression in rat liver and enhances oxidative phosphorylation capacity of liver mitochondria

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Identifiers

DOI

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10 April 2018

PubMed ID

11983456

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10 April 2018