Genetic Defects in E3 Component of α-Keto Acid Dehydrogenase Complexes
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Elsevier
Reference23 articles.
1. Multienzyme complexes
2. The mitochondrial glycine cleavage system
3. Molecular biology and biochemistry of pyruvate dehydrogenase complexes 1
4. Metabolic and Molecular Basis of Inherited Disease”;Robinson,1995
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