Gene therapy for organic acidemias: Lessons learned from methylmalonic and propionic acidemia

Organic acidemias (OA) are a group of rare autosomal recessive disorders of intermediary metabolism that result in a systemic elevation of organic acid. Despite optimal dietary and cofactor therapy, OA patients still suffer from potentially lethal metabolic instability and experience long‐term multi...

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Veröffentlicht in:Journal of inherited metabolic disease 2024-01, Vol.47 (1), p.63-79
Hauptverfasser: Chandler, Randy J., Venditti, Charles P.
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Sprache:eng
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