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. 2020 Feb 29;12:1179573520909377. doi: 10.1177/1179573520909377

Table 1.

Children with mitochondrial diseases who participated in the study.

1 8-year-old boy with TK2-related mitochondrial DNA depletion syndrome
2 6-year-old girl with TK2-related mitochondrial DNA depletion syndrome
3 7-year-old girl with MTTA-related mitochondrial myopathy
4 17-year-old girl with TMEM70-related mitochondrial complex V deficiency
5 9-year-old boy with NDUFS7-related Leigh syndrome
6 6-year-old girl with POLG-related Alpers disease
7 12-year-old boy with MTTK-related MERRF disease
8 8-year-old boy with MTPAP-related spastic ataxia
9 13-year-old boy with MTPAP-related spastic ataxia

Abbreviation: MERRF, myoclonic epilepsy with ragged red fibers.