Cлучай наследственного заболевания обмена веществ — дефицит ацил-КоА дегидрогеназы жирных кислот с очень длинной цепью (vlcad)
2013
The article presents the case of hereditary metabolic disease very long chain acyl-CoA dehydrogenase deficiency in a 14 years old child. It describes the clinical picture and development of the disease.
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