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Multiple Acyl-CoA Dehydrogenase Deficiency in an Infant

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Reference

  1. 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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Authors and Affiliations

  1. Department of Pediatrics, Newborn Medicine, Children’s Hospital, Capital Institute of Pediatrics, 2# Yabao Road, Beijing, China

    Xiao-ming Hu & Li Li

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  1. Xiao-ming Hu
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  2. Li Li
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Correspondence to Li Li.

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Source of Funding

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

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