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Pyruvate dehydrogenase e3-binding protein deficiency

Lipoamide dehydrogenase deficiency2-oxoglutarate complex deficiencyBranched chain alpha-ketoacid dehydrogenase complex deficiencyDiaphorase deficiencyDihydrolipoyl dehydrogenase deficiencyGlycine cleavage system L protein deficiencyPyruvate dehydrogenase protein X component deficiency
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Overview

Type of Disease: Genetic, autosomal recessive Pediatric onset

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FSHD Basics
Added On: Jul 15, 2019
Category: General
Language(s): English
A brief overview of the disease.