EDAF0CD3-C110-4B15-B421-501133E6F645Investigation of the function of the ER/mitochondria contact sites in cell physiology and diseaseIntramuralMC_UU_00015/7C008C651-F5B0-4859-A334-5F574AB6B57CMRCEXPENDITURE_ACTUAL15050003896FDC4-136E-407F-9773-5AA90A836D2EMutation in the MICOS subunit gene APOO (MIC26) associated with an X-linked recessive mitochondrial myopathy, lactic acidosis, cognitive impairment and autistic features.Journal of medical genetics3c426fa9278f4142bbc7070f949d5285Benincá C2021-01-01http://dx.doi.org/10.1136/jmedgenet-2020-10686132439808http://ukpmc.ac.uk/abstract/MED/324398080022-2593http://europepmc.org/abstract/MED/32439808583Journal Article/Review603d1d5a228a83.76807391