Synapse
⌘+K
Synapse
PulseExploreClubsResearchersJournals
Instagram
HomeClubsExplore
January 8, 1999Biochemical JournalOpen Access

Biochemical characterization of a variant human medium-chain acyl-CoA dehydrogenase with a disease-associated mutation localized in the active site

View Full Paper
Ask AI
Bookmark
Share

Authors

BKBurkhard KüchlerAAAbdel‐Ghany Abdel‐GhanyHelwan UniversityPBPeter BrossAarhus University

Discussion

Loading...

Member takes

Implication

Key Points

Key points are not available for this paper at this time.

Cite This Study

Küchler et al. (1999) studied this question.

synapsesocial.com/papers/6a9ed074d5bc2b984345486chttps://doi.org/10.1042/bj3370225
View Full Paper
Ask AI
Bookmark
Share

Also Consider

Synapse has enriched 4 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1Defects of metabolism of fatty acids in the sudden infant death syndrome.1985 · 122 citations
  2. 2Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene1992 · 81 citations
  3. 3Morbidity and mortality in medium chain acyl coenzyme A dehydrogenase deficiency.1994 · 98 citations
  4. 4Mechanisms of flavoprotein‐catalyzed reactions1989 · 568 citations