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Pataer A, Fang B, Yu R, Kagawa S, Hunt KK, McDonnell T, Roth JA, Swisher SG

Notably, NRF2 is a key molecule involved in the treatment of epilepsy with antioxidants

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Patients with SFXN4 mutations suffer from mitochondriopathies which result in heterogeneous clinical manifestations including respiratory defects in the musclem, deficits in neuro-motor integration and coordination, and/or anemia (Paul et al., 2019)

Assessment of risk factors and early presentations of Parkinson disease in primary care in a diverse UK population

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