DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Garcia-Diaz B, Barros MH, Sanna-Cherchi S. et al.
Infantile encephaloneuromyopathy and defective mitochondrial translation are due to a homozygous RMND1 mutation.
Am J Hum Genet 2012;
91 (04) 729-736
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