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  1. Jul 2024
  2. 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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    1. scibot 20 Jul 2024
      6326

      DOI: 10.1136/jmedgenet-2020-106861

      Resource: (BDSC Cat# 6326,RRID:BDSC_6326)

      Curator: @bandrow

      SciCrunch record: RRID:BDSC_6326

      What is this?
      DOI:10.1136/jmedgenet-2020-106861 RRID:BDSC_6326
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    ncbi.nlm.nih.gov/pmc/articles/PMC7116790/