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Up to: Hereditary neuromuscular disease · Congenital nervous system disorder · Inborn mitochondrial myopathy · X-linked recessive disease
X-linked recessive mitochondrial myopathy
A mitochondrial myopathy caused by defects in the MICOS subunit gene APOO (MIC26). Modelling in yeast and flies demonstrate an inability to insert MICOS complex into the inner mitohondrial membrane. Associated symptoms include, lactic acidosis, cognitive impairment and autistic features.
This condition has no sub-types.