Reference
Fu HX, Liu XY, Wang ZQ, et al. Significant clinical heterogeneity with similar ETFDH genotype in three Chinese patients with late-onset multiple acyl-CoA dehydrogenase deficiency. Neurol Sci. 2016;37:1099–105
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This work was funded by Capital Institute of Pediatrics, The Young Investigator grants (QN-15-03).
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Hu, Xm., Li, L. Multiple Acyl-CoA Dehydrogenase Deficiency in an Infant. Indian J Pediatr 86, 194–195 (2019). https://doi.org/10.1007/s12098-018-2768-z
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DOI: https://doi.org/10.1007/s12098-018-2768-z