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Dysregulated mitophagy and mitochondrial transport in severe inherited optic atrophy due to OPA1 mutations

Dysregulated mitophagy and mitochondrial transport in severe inherited optic atrophy due to OPA1 mutations

Dades bibliogràfiques
Autors principals: Poulton, J, Liao, C, Ashley, N, Morten, K, Phadwal, K, Williams, A, Feamley, I, Rosser, L, Lowndes, J, Fratter, C, Ferguson, D, Quaghebeur, G, Moroni, I, Bianchi, S, Lamperti, C, Macleod, L, Downes, S, Zeviani, M, Simon, A, Votruba, M
Format: Conference item
Publicat: 2012
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Ítems similars

  • Dysregulated mitophagy and mitochondrial transport in severe dominant optic atrophy due to OPA1 mutations
    per: Liao, C, et al.
    Publicat: (2012)
  • Dysregulated mitophagy and mitochondrial organization in optic atrophy due to OPA1 mutations.
    per: Liao, C, et al.
    Publicat: (2016)
  • Validating the RedMIT/GFP-LC3 mouse model by studying mitophagy in autosomal dominant optic atrophy due to the OPA1Q285STOP mutation
    per: Diot, A, et al.
    Publicat: (2018)
  • A Perspective on Accelerated Aging Caused by the Genetic Deficiency of the Metabolic Protein, OPA1
    per: Irina Erchova, et al.
    Publicat: (2021-04-01)
  • OPA1-related disorders: Diversity of clinical expression, modes of inheritance and pathophysiology
    per: Juan Manuel Chao de la Barca, et al.
    Publicat: (2016-06-01)

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