Back to matchesWe found a matchYour institution may have access to this item. Find your institution then sign in to continue.TitleTwo Novel Missense Mutations in Very Long Chain Acyl-CoA Dehydrogenase Deficiency.AuthorsBICHENG YANG; FENG WANGSubjectsINFANT disease diagnosis; INFANT disease treatment; DEHYDROGENASE genetics; PEDIATRICS; CASE studies; GENETIC mutation; ALGAE mutationPublicationIndian Pediatrics, 2018, Vol 55, Issue 3, p261ISSN0019-6061Publication typeCase Study