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The pyruvate dehydrogenase complex deficiency (PDCD) is a rare genetic neurometabolic disorder. It belongs to the group of mitochondrial diseases. Clinical manifestations range from often fatal, severe, neonatal lactic acidosis to serious neurologica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=57a035e5b1ae::5bb2ac25bb527a7e63016f3b8a534e05
https://doi.org/10.26800/lv-144-supl3-13
https://doi.org/10.26800/lv-144-supl3-13
