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Research Article

Non-viral mediated gene transfer of porphobilinogen deaminase into mammalian cells

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Pages 105-113 | Published online: 08 Jul 2009

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Delia D’Avola & Gloria Gonzalez Aseguinolaza. (2016) Prospect and progress of gene therapy in acute intermittent porphyria. Expert Opinion on Orphan Drugs 4:7, pages 711-717.
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Elena Pischik & Raili Kauppinen. (2015) An update of clinical management of acute intermittent porphyria. The Application of Clinical Genetics 8, pages 201-214.
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Articles from other publishers (4)

Helene J. Bustad, Juha P. Kallio, Marta Vorland, Valeria Fiorentino, Sverre Sandberg, Caroline Schmitt, Aasne K. Aarsand & Aurora Martinez. (2021) Acute Intermittent Porphyria: An Overview of Therapy Developments and Future Perspectives Focusing on Stabilisation of HMBS and Proteostasis Regulators. International Journal of Molecular Sciences 22:2, pages 675.
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R KAUPPINEN. (2005) Porphyrias. The Lancet 365:9455, pages 241-252.
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Annika Johansson, Grzegorz Nowak, Christer Möller, Pontus Blomberg & Pauline Harper. (2004) Adenoviral-mediated expression of porphobilinogen deaminase in liver restores the metabolic defect in a mouse model of acute intermittent porphyria. Molecular Therapy 10:2, pages 337-343.
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Annika Johansson, Christer Möller, Jens Fogh & Pauline Harper. (2004) Biochemical Characterization of Porphobilinogen Deaminase-Deficient Mice During Phenobarbital Induction of Heme Synthesis and the Effect of Enzyme Replacement. Molecular Medicine 9:9-12, pages 193-199.
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