DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Thompson K, Majd H, Dallabona C. et al.
Recurrent de novo dominant mutations inSLC25A4 cause severe early-onset mitochondrial disease and loss of mitochondrial DNA copy number.
Am J Hum Genet 2016;
99 (04) 860-876
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