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  1. Sep 2024
  2. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Development of a Bmi1+ Cardiac Mouse Progenitor Immortalized Model to Unravel the Relationship with Its Protective Vascular Endothelial Niche
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    ncbi.nlm.nih.gov/pmc/articles/PMC11354400/
  3. Jul 2024
  4. www.ncbi.nlm.nih.gov www.ncbi.nlm.nih.gov
    Original research: Mutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features
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    ncbi.nlm.nih.gov/pmc/articles/PMC7116790/
  5. May 2021
  6. www.sciencedirect.com www.sciencedirect.com
    Biallelic mutations in NDUFA8 cause complex I deficiency in two siblings with favorable clinical evolution
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    sciencedirect.com/science/article/pii/S1096719220302055