Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin-Reference-Cited by-同舟云学术

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Mitochondrial cytochrome deficiency presenting as a myopathy with hypotonia, external ophthalmoplegia, and lactic acidosis in an infant and as fatal hepatopathy in a second cousin

Published:1983-10 Issue:4 Volume:14 Page:462-470
ISSN:0364-5134
Container-title:Annals of Neurology
language:en
Short-container-title:Ann Neurol.

Author:

Boustany Rosemary N.,Aprille June R.,Halperin John,Levy Harvey

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference26 articles.

1. Morphologic features of hypermetabolic mitochondrial disease

2. A defect in pyruvate decarboxylase in a child with an intermittent movement disorder

3. Clinical Studies of a Patient With Pyruvate Decarboxylase Deficiency

4. Measurement of cytochromes in human skeletal muscle mitochondria, isolated from fresh and frozen stored muscle specimens

5. The Metabolism of Rat Brain Mitochondria

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4. Muscle Involvement and Restricted Disorders;Volpe's Neurology of the Newborn;2018

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