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2. Clinical and molecular characterisation of hereditary dopamine transporter deficiency syndrome: an observational cohort and experimental study

3. Mitochondrial physiology: Gnaiger Erich et al ― MitoEAGLE Task Group

4. Mitochondrial respiratory states and rates

5. HIBCH mutations can cause Leigh-like disease with combined deficiency of multiple mitochondrial respiratory chain enzymes and pyruvate dehydrogenase

10. 15.09 Inherited peripheral neuropathies: analysis of PDXK gene identifies a new treatable disorder

11. Infantile parkinsonism-dystonia due to dopamine transporter gene mutations: another genetic twist

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