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Multiple Acyl-CoA Dehydrogenase Deficiency in an Infant

  • Xiao-ming Hu
  • Li Li
Scientific Letter
  • 37 Downloads

Notes

Compliance with Ethical Standards

Conflict of Interest

None.

Source of Funding

This work was funded by Capital Institute of Pediatrics, The Young Investigator grants (QN-15-03).

Reference

  1. 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;37:1099–105CrossRefPubMedGoogle Scholar

Copyright information

© Dr. K C Chaudhuri Foundation 2018

Authors and Affiliations

  1. 1.Department of Pediatrics, Newborn Medicine, Children’s HospitalCapital Institute of PediatricsBeijingChina

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