KEARNS-SAYRE SYNDROME WITH MUSCLE MITOCHONDRIAL DNA DELETION
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference3 articles.
1. Progressive cytochrome C oxidase deficiency in a case of Kearns-Sayre syndrome: Morphological, immunological, and biochemical studies in muscle biopsies and autopsy tissues;Bresolin;Ann Neurol,1987
2. The clinical features of mitochondrial myopathy;Petty;Brain,1986
3. Deletions of muscle mitochondrial DNA in patients with mitochondrial myopathies;Holt;Nature,1988
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