Mitochondrial disease in pregnancy: a systematic review. - Wikidata - awgldk - TriplyDB

Mitochondrial disease in pregnancy: a systematic review.

Mitochondrial disease in pregnancy: a systematic review.

http://www.wikidata.org/entity/Q37185909

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Monogenic diabetes and pregnancy Management of pregnancy in cardiomyopathies and heart failure.

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P2860

Mitochondrial disease in pregnancy: a systematic review.

http://www.wikidata.org/entity/Q37185909

description

article científic

@ca

article scientifique

@fr

articolo scientifico

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artigo científico

@pt

bilimsel makale

@tr

scientific article published on 23 June 2011

@en

vedecký článok

@sk

vetenskaplig artikel

@sv

videnskabelig artikel

@da

vědecký článek

@cs

name

Mitochondrial disease in pregnancy: a systematic review.

@en

Mitochondrial disease in pregnancy: a systematic review.

@nl

type

label

Mitochondrial disease in pregnancy: a systematic review.

@en

Mitochondrial disease in pregnancy: a systematic review.

@nl

prefLabel

Mitochondrial disease in pregnancy: a systematic review.

@en

Mitochondrial disease in pregnancy: a systematic review.

@nl

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Obstetric medicine

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Mitochondrial disease in pregnancy: a systematic review.

@en

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D M Turnbull

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H E Turnbull

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R E Say

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R W Taylor

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P2860

Thymidine phosphorylase gene mutations in MNGIE, a human mitochondrial disorder

MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion

Deficiency of the ADP-forming succinyl-CoA synthase activity is associated with encephalomyopathy and mitochondrial DNA depletion

Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics.

Mutant POLG2 disrupts DNA polymerase gamma subunits and causes progressive external ophthalmoplegia

Deficiency of the alpha subunit of succinate-coenzyme A ligase causes fatal infantile lactic acidosis with mitochondrial DNA depletion

Mutations of ANT1, Twinkle, and POLG1 in sporadic progressive external ophthalmoplegia (PEO)

The deoxyguanosine kinase gene is mutated in individuals with depleted hepatocerebral mitochondrial DNA

Mutant mitochondrial thymidine kinase in mitochondrial DNA depletion myopathy

Atypical MELAS syndrome associated with a new mitochondrial tRNA glutamine point mutation.

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90-94

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scholarly article

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10.1258/OM.2011.110008

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3

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Roger Whittaker

Robert McFarland

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2011-06-23T00:00:00Z

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