DOI: 10.1055/s-00029030

Journal of Pediatric Neurology

References

Janer A, Antonicka H, Lalonde E. et al.
An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect.

Am J Hum Genet 2012;
91 (04) 737-743

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