Thus, mutant ATAD3A was linked to neurological syndromes (Harel et al., 2016), mutant TAZ in the Barth syndrome (Bione et al., 1996), while the Mic13 deficiency was c,orrelated to mitochondrial hepato-encephalopathy (Kishita et al., 2020). The gene discussed is MICOS13; the disease is Barth syndrome.