Mitochondrial myopathy: a genetic study of 71 cases (Q24522304)

Europe PubMed Central

title

Mitochondrial myopathy: a genetic study of 71 cases (English)

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main subject

mitochondrial myopathy

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Journal of Medical Genetics

inferred from title

author

John A. Morgan-Hughes

series ordinal

3

object named as

J A Morgan-Hughes

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author name string

A E Harding

series ordinal

1

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R K Petty

series ordinal

2

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language of work or name

English

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publication date

August 1988

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published in

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volume

25

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issue

8

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page(s)

528-35

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cites work

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12 December 2020

Myoclonus, cerebellar disorder, neuropathy, mitochondria1 myopathy, and ACTH deficiency

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Fatal infantile mitochondrial myopathy due to cytochrome c oxidase deficiency

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Immunological abnormalities in a family with progressive external ophthalmoplegia

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Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies

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Lipid storage myopathy in familial hyperlipoproteinemia

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Mitochondrial myopathies

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Late-onset hereditary myopathy with abnormal mitochondria and progressive dementia

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Familial Myopathy With Abnormal Muscle Mitochondria

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12 December 2020

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Familial association of metabolic myopathy, lactic acidosis and sideroblastic anemia

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Familial progressive external ophthalmoplegia with abnormal muscle mitochondria

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Hereditary mitochondrial myopathy with lactic acidemia, a De Toni-Fanconi-Debré syndrome, and a defective respiratory chain in voluntary striated muscles

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A mitochondrial myopathy with a deficiency of respiratory chain NADH-CoQ reductase activity

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Histochemical and ultrastructural analysis of the mitochondrial changes in a familial mitochondrial myopathy

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Myopathies with abnormal mitochondria. A clinical, histological, and electrophysiological study

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Crossref

https://api.crossref.org/works/10.1136%2FJMG.25.8.528

7 January 2021