MGME1 This gene, previously known as C20orf72, encodes a RecB-type exonuclease belonging to the PD-(D/E)XK nuclease superfamily [ 76 ].
[mdpi.com]
[…] mitochondrial disease include ptosis, external ophthalmoplegia, proximal myopathy and exercise intolerance, cardiomyopathy, sensorineural deafness, optic atrophy, pigmentary retinopathy
[raredr.com]
Tremor 2, 8, 12 15, 21, 27 Parkinsonism 3, 9, 12, 17 2, 21 Dystonia 3 17 Ocular disorders Ophthalmoplegia 3, 2, 1, 9 Nystagmus 1, 3, 6 Slow saccades 2 1, 3, 7, 17 Pigmentary retinopathy
[neuromuscular.wustl.edu]