Mutations in electron transfer flavoprotein (ETF) and its dehydrogenase (ETFDH) are the molecular basis of multiple acyl-CoA dehydrogenation deficiency (MADD), an autosomal recessively inherited and clinically heterogeneous disease that has been divided into three clinical forms: a neonatal-onset fo
✦ LIBER ✦
Metabolic effects of carnitine medication in a patient with multiple acyl-CoA dehydrogenation deficiency
✍ Scribed by N. Gregersen; M. Fjord Christensen; S. Kølvraa
- Publisher
- Springer
- Year
- 1985
- Tongue
- English
- Weight
- 235 KB
- Volume
- 8
- Category
- Article
- ISSN
- 0141-8955
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