Oxidative phosphorylation defect associated with primary adrenal insufficiency
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference21 articles.
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3. Bilateral infantile cataractogenesis in a patient with deficiency of complex I, a mitochondrial electron transport chain enzyme;Ciulla;J Pediatr Ophthalmol Strabismus,1995
4. Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies;Zheng;Biochim Biophys Acta,1990
5. Molecular analysis of oxidative phosphorylation diseases: mitochondrial DNA mutation detection;Shoffner,1995
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