Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy - Concepedia

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Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy

DOI Full Paper Access

147

Citations

0

References

1977

Year

B. H. Robinson, Jennifer Taylor, W. G. Sherwood

Pediatric Research

Metabolic DiseasePhysiologyInherited Metabolic DiseasePediatricsDihydrolipoyl Dehydrogenaseα-Ketoglutarate Dehydrogenase ComplexesMetabolismMedicineHuman Lactation

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