Multiple Acyl-CoA Dehydrogenase Deficiency in an Infant

Indian J Pediatr. 2019 Feb;86(2):194-195. doi: 10.1007/s12098-018-2768-z. Epub 2018 Aug 20.

Authors

Xiao-Ming Hu¹, Li Li²

Affiliations

¹ Department of Pediatrics, Newborn Medicine, Children's Hospital, Capital Institute of Pediatrics, 2# Yabao Road, Beijing, China.
² Department of Pediatrics, Newborn Medicine, Children's Hospital, Capital Institute of Pediatrics, 2# Yabao Road, Beijing, China. lili1010@sina.com.

PMID: 30128629
DOI: 10.1007/s12098-018-2768-z

No abstract available

Publication types

Case Reports
Letter

MeSH terms

Base Sequence
Child, Preschool
DNA Mutational Analysis
Female
Humans
Infant, Newborn
Male
Multiple Acyl Coenzyme A Dehydrogenase Deficiency / blood
Multiple Acyl Coenzyme A Dehydrogenase Deficiency / genetics*
Mutation
Open Reading Frames / genetics