Publication | Closed Access
The mitochondrial 13513G>A mutation is associated with Leigh disease phenotypes independent of complex I deficiency in muscle
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Citations
21
References
2008
Year
Mitochondrial MyopathyMitochondrial FunctionGenetic DisorderMedicineGeneticsLeigh DiseasePathologyMolecular GeneticsNeuromuscular PathologyMitochondrial 13513G
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