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Michele Brischigliaro

University of Padua

5

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28

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Modelling of BCS1L-related human mitochondrial disease in Drosophila melanogaster

2021 Journal of Molecular Medicine
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Cytochrome c oxidase deficiency.

2021 Biochimica et Biophysica Acta
- Michele Brischigliaro
- Massimo Zeviani
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Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features.

2020 Journal of Medical Genetics
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Knockdown of APOPT1/COA8 Causes Cytochrome c Oxidase Deficiency, Neuromuscular Impairment, and Reduced Resistance to Oxidative Stress in Drosophila melanogaster

2019 Frontiers in Physiology
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