1.11.a

Disorders of mitochondrial shuttles and carriers

  • Mitochondrial citrate carrier deficiency (Combined D-2- and L-2-hydroxyglutaric aciduria)
  • Mitochondrial phosphate carrier deficiency
  • Adenine nucleotide translocator deficiency (Mitochondrial DNA depletion syndrome type 12 (cardiomyopathic type); adPEO with mitochondrial DNA deletions type 2)
  • Mitochondrial dicarboxylate transporter deficiency
  • Mitochondrial oxoglutarate/malate carrier deficiency (Hereditary paraganglioma syndrome type 6)
  • Mitochondrial aspartate-glutamate carrier isoform 1 deficiency (Early infantile epileptic encephalopathy type 39; aralar deficiency)
  • Mitochondrial aspartate aminotransferase deficiency
  • Cytosolic malate dehydrogenase deficiency
  • Cytosolic glycerol-3-phosphate dehydrogenase deficiency (Transient infantile hypertriglyceridemia)
  • Mitochondrial oxodicarboxylate carrier deficiency
  • Mitochondrial glutamate transporter deficiency (Early infantile epileptic encephalopathy type 3)
  • Mitochondrial ATP-Mg/phosphate transporter deficiency (Gorlin-Chaudhry-Moss syndrome; Fontaine syndrome)
  • S-adenosylmethionine carrier deficiency (Combined oxidative phosphorylation deficiency type 28)
  • Mitochondrial glycine transporter deficiency (Congenital sideroblastic anemia type 2)
  • Mitochondrial calcium uniporter deficiency (Myopathy with extrapyramidal signs)
  • Mitochondrial calcium uniporter 2 deficiency

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