(Q70499040)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6434847%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

Mitochondrial myopathies: disorders of the respiratory chain and oxidative phosphorylation (English)

1 reference

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11 October 2019

author

John A. Morgan-Hughes

3

object named as

J A Morgan-Hughes

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11 October 2019

author name string

J B Clark

1

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11 October 2019

D J Hayes

2

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11 October 2019

E Byrne

4

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11 October 2019

publication date

1 January 1984

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Journal of Inherited Metabolic Disease

11 October 2019

published in

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11 October 2019

volume

7 Suppl 1

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11 October 2019

page(s)

62-68

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https://scigraph.springernature.com/pub.10.1007/bf03047377

11 October 2019

exact match

0 references

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Pyruvate Dehydrogenase Phosphatase Deficiency: A Cause of Congenital Chronic Lactic Acidosis in Infancy

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Multiple genotypes, multiple phenotypes, and partial defects

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Mitochondrial myopathies

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Fatal infhntile mitochondrial myopathy and renal dysfunction due to cytochrome-c-oxidase deficiency

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Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

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12 December 2020

Identifiers

DOI

10.1007/BF03047377

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6434847%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference