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In addition to components of the PDHc itself, mutations in the gene (PDP1) encoding one of the catalytic subunits of the major PDH phosphatase and mutations in the gene (PDHX) that encodes a E3 subunit binding protein, have been shown to be associated with PDH deficiency syndromes

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[DOI] [PubMed] [Google Scholar] 104.Szabo S., Sandor Z

Questions to Ask the Prescribing Clinician If you proceed and connect with a licensed provider through TeleHealth Med, these are the questions worth raising